HYDROXYETHYCELLULOSE GEL COMPOSITION COMPRISING BACTERIOPHAGES

Abstract

The present invention provides a hydrogel comprising hydroxyethyl cellulose (HEC) and bacteriophages.

Claims

1. A hydrogel comprising hydroxyethyl cellulose (HEC) and bacteriophages.

2. The hydrogel of claim 1, further comprising CaCl.sub.2 and glycerol.

3. The hydrogel of claim 1, wherein the hydrogel comprises 10% to 33% CaCl.sub.2.

4. The hydrogel of claim 2, wherein the hydrogel comprises 6% to 22% glycerol.

5. The hydrogel of claim 1, wherein the hydrogel comprises 3% to 10% HEC.

6. The hydrogel of claim 1, wherein the concentration of the bacteriophages is from 10.sup.2 pfu/ml to 10.sup.8 pfu/ml.

7. The hydrogel of claim 1, comprising 10.sup.2 pfu/ml to 10.sup.8 pfu/ml bacteriophages, 3 to 10% HEC, 10 to 33% CaCl.sub.2, and 6 to 22% glycerol.

8. (canceled)

9. The hydrogel of claim 1, further comprising a buffer.

10. The hydrogel of claim 1, wherein the hydrogel has a pH of 7.0 to 7.8.

11. The hydrogel of claim 1, wherein the hydrogel has a viscosity of 1000 mPas up to 100.000 mPas.

12. (canceled)

13. A lyophilizate of the hydrogel of claim 1.

14-22. (canceled)

23. A method of preparing a hydrogel comprising hydroxyethyl cellulose (HEC) and bacteriophages comprising the steps of a) providing HEC in a solid state of matter, b) dissolving solid HEC of step a) in a liquid component comprising water and bacteriophages, and c) optionally adding water until the desired viscosity is reached.

24. A method of treating and/or preventing a bacterial infection in a subject in need thereof, comprising administering to the subject and effective amount of the hydrogel or the lyophilizate of the hydrogel of claim 1.

25. The method of claim 24 wherein the subject has been identified as suffering from a bacterial infection and the hydrogel or the lyophilizate is administered to the identified subject.

26. (canceled)

27. The method of claim 24, wherein the hydrogel or the lyophilizate of the hydrogel is applied to the subject during surgery of the subject.

28. The method of claim 24, wherein the hydrogel or the lyophilizate of the hydrogel is applied to a surgical site, an implant, an anastomosis, a wound, an abrasion, a cut, a stab, a non-intact skin tissue and/or mucosal tissue, an entrance point of a catheter, a covering of sterile material, a wound and/or implant coverage, and/or suture material.

29. The method of claim 24, wherein the hydrogel or the lyophilizate of the hydrogel is used to treat and/or prevent a bacterial infection associated with an implant.

30. The method of claim 24, wherein the hydrogel or the lyophilizate of the hydrogel is directly applied to a surface of the implant, either outside of a subject's body or in a subject's body.

31-33. (canceled)

34. The method of claim 24, wherein the hydrogel or the lyophilizate of the hydrogel is applied to a surface of a subject's body or to a surface of an implant manually and/or using one or more helping devices, preferably one for more syringes, needles and/or catheters.

35. The method of claim 24 wherein the subject is a human.

Description

FIEGURE LEGENDS

[0204] FIG. 1: Na-Hyaluronat gel on filter before stored for 24 h at 37? C. The gel is much too firm to be spread well on the filter paper and shows an agglomerate as a result of the stiffness of the gel.

[0205] FIG. 2: Na-Hyaluronat gel on skin: the gel shows stiffness even on the skin. Tries of application and spreading on the shown arm were painful, due to the firm condition of the gel.

[0206] FIG. 3: Carbomer gel on skin: the gel shows a highly adhesive character. Spreading on the skin difficult. Moreover, application and spreading was painful, due to the stickiness. A wanted layer of gel has not been applicable.

[0207] FIG. 4: Carbomer gel: to show the stickiness of the carbomer gel a bit of gel has been taken between two fingers. The fingers then has been spread. As result the gel sticked to the fingers and got thinner in the middle. So it has been show that application was too difficult and the gel is too adhesive.

[0208] FIG. 5: HEC gel on filter before stored for 24 h at 37? C.: the gel shows a solid character and a good spread-ability/possibility of application at the same time.

[0209] FIG. 6: HEC gel on skin: on skin the application has been tested. The application has been very easy. Moreover, a wanted layer of gel has been possible to applicate.

[0210] FIG. 7: HEC gel after 24 h at 37? C.: the gel has been dried by the storage-conditions. The solid character after the storage, without any packaging protecting the gel from water evaporation, shows the essential of adequate primary packing. Moreover, the gel stayed in the form in which was stored showing an ongoing coverage of the application area.

[0211] FIG. 8: Polaxamer gel after 24 h at 37? C., the gel has been dried by the storage-conditions. The solid character after the storage, without any packaging protecting the gel from water evaporation, shows the essential of adequate primary packing. The gel did not stay in the form in which was stored showing a change in the coverage of the application area and a transformation into a cube-like form.

[0212] FIG. 9: Na-Hyaluronat gel after 24 h at 37? C.: the gel has been dried by the storage-conditions. The solid character after the storage, without any packaging protecting the gel from water evaporation, shows the essential of adequate primary packing. Moreover, the gel did not stay in the form in which was stored showing a change in the coverage of the application area. Stickiness has increased with the loss of water.

[0213] FIG. 10: HEC gel after sterile manufacturing: direct loading method, Ph. Eur. 2.6.1, showing no sign of bacterial contamination after a prolonged testing to increase the probability of detection.

[0214] FIG. 11: Plaques could still be detected after steam sterilization of Phages: On a standardized bacterial bio burden phages has been spread out after steam sterilization. After the time of incubation plaques show that phages have survived the steam sterilizing process and are still active.

[0215] FIG. 12: Sterile preparation of HEC gel: The FIG. 12 shows the sterile result of the combination of phages and gel.

[0216] FIG. 13: Gel after steam sterilisation: direct loading method of Ph. Eur 2.6.1, showing no sign of bacterial contamination after a prolonged testing to increase the probability of detection.

[0217] FIG. 14: Preoperative PET-CT. Representative slides from the pre-operative [F18] fluorodeoxyglucose PET-CT scan. The enhancement as the level of accumulation of the tracer substance around the stent-graft in the thoracic aorta is a sign of active inflammation.

[0218] FIG. 15: Intraoperative images from the first step of treatment: The descending aorta has been mechanically debrided from periaortic infectious tissue

[0219] FIG. 16: Intraoperative images from the first step of treatment: Two endo-sponges had been placed around the aorta.

[0220] FIG. 17: Intraoperative images from the first step of treatment: Finally, another vacuum sponge was applied for ventral coverage of the aorta (C) before the thorax was closed.

[0221] FIG. 18: Off-the-shelf release of an aortic stent graft system and manual surface covering with bacteriophages gel.

[0222] FIG. 19: Lateral X-Ray after stent implantation, showing a complete overcovering of the infected stent graft by the new ones.

[0223] FIG. 20: PET-CT three months after implanting the bacteriophage gel covered stent showing no revealing signs of infection in and around the thoracic aorta.

[0224] FIG. 21: PET-CT showing the infected aortic-bi-femoral vascular graft with right femoral tissue infection.

[0225] FIG. 22: Impressions of the surgical procedures and the application of the bacteriophages gel

[0226] FIG. 23: PET-CT three months post intervention without signs of infection enclosing the aorta or both femoral regions

[0227] FIG. 24: Exemplary pictures of lyophilized hydrogels.

[0228] FIG. 25: Preparation of lyophilizates from bacteriophage comprising hydrogels.

[0229] FIG. 26: Four lyophilizated hydrogels centered on agar plates with Staphylococcus aureus.

[0230] FIG. 27: Bacteria-free (circled) plaques on the culture medium.

[0231] FIG. 28: Experimental setup.

[0232] FIG. 29: Data of release of bacteriophages from the products B1, B2, C1 and C2 over time of Example 5: x-axis showing bacteriophage (BPh) concentration in [pfu/ml] and y-axis showing time in [min].

[0233] FIG. 30: Hurley II/III in left axilla (left picture) and Hurley II/III right gluteal (right picture).

[0234] FIG. 31: Surgical treatment of the left axilla comprising administration of a hydrogel comprising HEC and bacteriophages. First, the left axilla received local anaesthesia (top left) followed by surgical removal of the affected tissue (surgical access left axilla, top right), bacteriophage and carrier application (bottom left) and subsequent skin suture of the axilla (bottom right).

[0235] FIG. 32: Axilla status after 2 weeks (left) and 10 weeks (right).

[0236] FIG. 33: Gluteal status after 2 weeks (top) and 10 weeks (bottom).

[0237] FIG. 34: Wound seize reduction over time with the x-axis showing the time and the y-axis indicating wound seize.

EXAMPLE 1

Finding a Suitable Phew Containing Gel-Galenic for Clinical Use: a Laboratory Trail

Abstract

[0238] In vitro laboratory tests were carried out to find a suitable basis-gel for the PhaTEC Phages Gel-Product. The shortlist of gel formers included Hydroxy-Ethyl-Cellulose (=HEC), Sodium-Hyaluronate, Polaxamer, Carbomer and Silicon dioxide (=SiO.sub.2 [highly dispersed]). Testing was performed according to spreadability on filter paper and on the skin, the haptics and sensory properties, as well as the gel consistency and the behavior after 24 h at 37? C. As bacteriophages we used a cocktail of different Bacteriophages (SniPha 360) which can be purchased from the company Phage24 in Austria. The requirements are placed on the gel, which is to become the subsequent basis of the PhaTEC Product. All tests were carried out under sterile conditions in the laboratory of Pohl-Boskamp GmbH & Co. KG, taking GLP (good laboratory practice) into account.

[0239] With regard to sterilization, in our experiments various methods are shown that lead to a sterile product of the HEC gel and the phage cocktail.

[0240] Furthermore, both the HEC gel and the phages can be steam sterilized. Thus, the PhaTEC product, containing the gel and phages, can be sterilized in the final container for easy and cost-effective industrial production.

1. Background

1. Stability and Spreadability

[0241] The PhaTEC product is to be used for intra- and extra-corporal application. Among other things, the product is to be applied to mucous and skin areas, wounds and surgical sites such as anastomoses. For this purpose, an appropriate spreadability is required (to cover an application area) with simultaneous product stabilityfor example, to generate/apply an individual layer thickness and to remain at the place of application. Moreover, the gel should be spreadable so that it can be applied easily and painlessly to sensitive areas such as fresh wounds. In addition, cooling is desirable, especially in the case of extra-corporeal application, in order to counteract inflammatory reactions and to provide a pleasant feeling on the application area.

2. Possibility of Sterilization

[0242] Due to the pursuit of a product that is intended for extra- as well as intra-corporeal application, the product and thus the initial components, such as the base gel, have to provide the possibility of sterility.

3. AdequateSspreading Around the Place of Application

[0243] The gel should be reduced in viscosity by the introduction of skin or body temperature and body water, so that the phages contained later are released over a defined time. This results in a prolonged release of the therapeutic agent, which does not affect the body, due to the degradation of the product by dilution and physiological excretion processes.

4. Feeling on the Skin

[0244] To all medical, as well as pharmaceutical requirements, the acceptance of the patient is essential. Since the phages do not cause any physical reactions and have no side effects, the gel, which the patient feels, especially when applied cutaneous/extra-corporal, must be pleasant on the skin and/or mucous membrane.

2. Gel-Manufacturing

[0245] Initially, all gels were prepared with a gel former content of 13%. The Carbomer, Na-hyaluronate and HEC gels were the easiest to prepare.

[0246] From the five preparations, only three solid gels were obtained:

[0247] HEC-, Carbomer- and Sodiumhyaluronate-Gel. The Silicon dioxideat the applied concentrationformed a viscous liquid but not a solid gel and did not dissolve completely. The Polaxamer showed gel-islands that were not connected with each other; in addition, much water was not absorbed (FIG. 1)

3. Haptic/Sensory Skin Testing

Methods:

[0248] Different Gel-formations had been tested at the skin surface of the same test person. Sensitive feeling as far as skin reaction had been observed.

[0249] The Na-hyaluronate (Natriumhyaluronat EP) gel was much too firm to be spread well on the filter paper. FIG. 1

[0250] On the skin, especially on hairy skin areas such as the arm used in the test, application and spreading was painful, due to the firm condition. FIG. 2

[0251] The Carbomer (Carbomer EP, Carboprol 71 G) gel was highly adhesive and therefore difficult to spread on the filter paper and almost impossible to spread on the skin. Moreover, on the skin, especially on hairy skin areas such as the arm used in the test, application and spreading was painful, due to the stickiness: FIG. 3, FIG. 4

[0252] The HEC (Natrosol 250 HX) gel felt the most pleasant: It was easily spreadable on the filter paper and on the skin with a simultaneous firmness that allowed application of individual layer thicknesses: FIG. 5, FIG. 6

Results:

[0253] The feeling of the gels proved to be very different: The gels showed very different characteristics: If the SiO.sub.2 (hochdisperses Siliciumdioxid; Aeroperl 300 Pharma) and Polaxamer (Polaxamer 407) gel were not tested on the filter paper and/or skin due to the liquid state of the SiO.sub.2 gel and due to the island formation of the Polaxamer gel, the Carbomer gel was found to be highly adhesive and difficult to apply because of the free flowing properties. The stickiness of the Carbomer gel was very unpleasant when applied to the skin and painful in hairy areas, such as (in the test) the arm. The cooling effect was almost immediately noticeable. The gel, especially on the skin, did not remain at the application site and immediately flowed undirected and uncontrolled into the surrounding area. An appropriate layer thickness could not be applied.

[0254] The Sodiumhyaluronate gel was much too firm for painless, simple application: It could hardly be spread on the filter paper and on the skin, especially in hairy areas, such as (in the test) the arm, it was painful and difficult to spread due to its firmness.

[0255] Hard, but still easy and painless to apply and remaining at the application site as desired, was the HEC gel: Here, it was not only possible to demonstrate good spreadability on the filter paper and on the skin; the feeling on the skin was also pleasant. Application on the skin was simple and painless. The gel distribution could be done individually with regard to the desired layer thickness. The cooling effect occurred after some time due to the applied layer thickness. In addition, the applied gel layer gave a feeling of a protective layer, like a plaster or similar.

4. Gel-Galenic Behavior Under Drying Conditions

[0256] The heat exposure of 37? C. was carried out by means of a drying oven. In order to test the cooling effect desired when external applied, the gels (10 ml each) were placed in the center of a filter paper and the border was marked. The gels were stored at 37? C. for 24 h in order to demonstrate the drying of the gels and thus a cooling effect due to evaporative cooling.

Methods:

[0257] The haptic/sensory test after 24 h at 37? C. was performed with gels that were in cups with the lid on in the drying cabinet. FIG. 7, FIG. 8, FIG. 9

Results:

[0258] The primary packaging provided adequate protection against dehydration. Under physiological conditions, the product is liquefied by the interstitial water and physiologically degraded.

5. Sterility

5.1. Sterile Production

5.1.1. Gel

Methods:

[0259] The gel was sterilely prepared in laboratory-scale tests. For this purpose, previously sterilized equipment and a Bench (laminar air flow) were used. The prepared HEC gel was tested according to the direct loading method of Ph. Eur 2.6.1.(FIG. 5).

Results:

[0260] No bacterial growth after 24 h until 9 days, when the extended test was ended. No microbial growth was evident over the entire period. FIG. 10

5.1.2. Phages

[0261] It is a defined objective of PhaTEC that its phage products can be produced industrially, standardized and easily. A major aspect of a simple, industrial production is the sterilization of the product in the final container. Two possibilities of sterilization of the gel are described above and have been verified by the corresponding tests. The phages can be sterilized via sterile filtration, as tested and described earlier.

Methods:

[0262] Phages were sterile-filtered and showed no bacterial growth on different culture media after 24, 48 and 72 h at 37? C. The cocktail was tested positive on an E. coli bacteria culture on agar, Samples of the phage cocktail, containing about 10.sup.7 pfu/ml, were steam sterilized and carried out the test with the steam sterilized BPG against the same bacterial strain on fresh corresponding agar.

Results:

[0263] Plaques could be detected, approx. 6?10{circumflex over ()}2 PFU/ml. That leads to the result, that steam-sterilized bacteriophages from our phage cocktail still have lytic activity against the corresponding bacterial strain. FIG. 11

[0264] In conclusion it has been demonstrated, that Steam-sterilization of phages is possible.

5.2. Steam Sterilization

5.2.1. Gel

Methods:

[0265] The gel was prepared, in addition to sterile manufacture, in a normal laboratory clean setting and steam sterilized in the final container. FIG. 12

Results:

[0266] The steam sterilized HEC gel showed no growth over the entire time when tested as described under Sterile Preparation. FIG. 13

6. Summary

[0267] Among the most suitable gel formers tested, Hydroxy-Ethyl-Cellulose is the best gel former: the haptic, the good, uniform, even protective feel on the skin, as well as the properties of easy application, also in terms of a desired layer thickness, are just some of the aspects that lead to this result.

[0268] With regard to sterilization, there are various methods shown that lead to a sterile product of the HEC gel and the phage cocktail. All individual tests lead to the conclusion that all methods and procedures, presented above, are suitable to bring the PhaTEC Product into a sterile state.

[0269] Furthermore, both the HEC gel and the phages can be steam sterilized. Thus, the PhaTEC product, containing the gel and phages, can be sterilized in the final container for easy and cost-effective industrial production.

EXAMPLE 2

[0270] Successful treatment of an infected TEVAR with extra- and endovascular bacteriophage application

Abstract

[0271] Objectives: Graft infections are severe complications in vascular surgery. Surgical resection of infected aortic stent-grafts is associated with high mortality and morbidity. Therefore, alternatives to inadequate antibiotic treatment and extensive surgery are urgently needed.

Case

[0272] A 67-years-old woman was admitted with an infected stent-graft in the thoracic aorta. Local infection was confirmed by PET-CT imaging. Due to comorbidities, surgical resection of the stent-graft was not feasible. Therefore, a three-step approach for local bacteriophage treatment was performed as a last-resort treatment. First, the para-aortic tissue was debrided via left thoracotomy, a bacteriophage suspension was applied around the aorta and an irrigation-vacuum-system was installed. After repeated alternating instillation of the bacteriophage suspension for three days, as the second step vacuum sponges were removed and a bacteriophage-containing gel was locally applied locally around the aorta. In the third step, the bacteriophage-containing gel was applied to a thoracic stent-graft, which in turn was endovascularly placed into the infected stent. After 28 days, the patient was discharged from hospital with normalized infection parameters. PET-CT imaging at three months post intervention did not show signs of infection in or around the thoracic aorta.

Conclusions

[0273] This case demonstrates successful treatment of an infected endovascular stent-graft by application of bacteriophages both to extravascular and, as a novel approach, endovascular sites using a bacteriophage-coated stent-graft. This success was only possible due to the hydrogel comprising HEC and bacteriophages according to the first aspect of the present invention, which allowed localization of phages in situ at the site of infection as well as continuous bacteriophage release in a retarded manner.

Keywords staphylococcus aureus sepsis, graft infection, phage therapy, antibiotic resistance

Background

[0274] In vascular surgery, infections of vascular grafts are severe complications. Especially infections of endovascular aortic stent-grafts are associated with a high morbidity and mortality up to 75%. Since these endovascular procedures are often performed in older patients with multiple comorbidities who do not qualify for open aortic repair, the required removal of the infected stent-grafts and in situ reconstruction with autologous tissue or extra-anatomic replacement are related with early postoperative morbidity and mortality over 20%. Even with successful treatment, the reinfection rate is up to 20%.

[0275] Bacteria embedded into the pen-prosthetic tissue form a surface-adherent biofilm and therefore have a up to 1000-fold greater tolerance to antibiotics. Vice versa, even targeted antibiotic treatment can only suppress a stent-graft infection and is no curative treatment option.

[0276] In order to reduce the morbidity and mortality of the unavoidable surgical treatment, alternative less invasive approaches are urgently needed. In this context, bacteriophages and their bacteriolytic activities are a promising therapeutic option.

Case

[0277] In August 2020, a 67-year-old female patient was admitted to the hospital due to worsening general condition and thoracic respiratory pain. There was a pronounced cough with deep inspiration, without sputum, and fever up to 38.6? C. Infection with Sars-CoV-2 was ruled out. The patient showed a leukocyte count of 16.7?10.sup.9/l and a serum C-reactive protein value of 199.6 mg/l. Secondary findings included a condition after thoracoabdominal stent graft implantation (COOK stent 34/152 mm) after Stanford type-B aortic dissection in February 2009. Furthermore, the patient suffered from Osler disease that required prednisolone treatment, condition after lung artery embolism, arterial hypertension, an atrophic left kidney and diverticulosis of the sigmoid colon.

[0278] Chest X-ray showed no evidence of pneumonia. Antibiotic therapy with ampicillin/sulbactam and roxithromycin was started. After Staphylococcus aureus was detected in the blood culture, antibiotic therapy was switched to Flucloxacillin and after five days, to cefuroxime due to an allergic skin eczema.

[0279] Endocarditis was ruled out. The patient showed progression of known leukocytoclastic vasculitis with involvement of both legs, arms, cleavage, hands, and soles without involving the kidneys. Cutaneous symptoms improved with intensed prednisolone therapy. The progression of vasculitis was considered a reaction to the systemic infection. The antibiotic treatment was switched to meropenem and cefazolin.

[0280] A computed tomography scan of the chest and abdomen did not reveal infection foci. To rule out the aortic stent graft as a focus of infection, a fluorodeoxyglucose PET-CT was performed.

[0281] As a result, pathologically increased metabolic activity of the entire proximal aortic stent was visualized, beginning at the level of the mid-aortic arch and extending to the level of the eighth thoracic vertebra as a sign of florid stent infection. Additionally, inflammatory mediastinal soft tissue swelling and left pleural effusion were described. FIG. 14.

[0282] Due to the bad condition and several comorbidities of the patient, the surgical resection of the infected stent-graft and autologous anatomical reconstruction were not feasible. The patient herself whished an alternative to indefinite systemical antibacterial treatment. Therefore, an experimental approach using local bacteriophage application was planned as a last resort treatment according to Article 37 of the Declaration of Helsinki in accordance with the local ethics committee (A 2021-0132).

Bacteriophage Treatment

[0283] As a curative therapeutic strategy a three-step approach for both extra- and endovascular application of SniPha 360 (Phage24.com, Austria) was performed. SniPha 360 is a commercially available cocktail of lytic bacteriophages against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Streptococcus pyogenes, Proteus vulgaris and Proteus mirabilis.

[0284] After the risks and benefits of the experimental procedure were explained, the patient consented to the therapy. First, the extravascular treatment was performed by left-sided thoracotomy. The visceral pleura was found to adhere to the aorta. After obtaining local swab specimens for microbilogical analysis, debridement and jet-lavage were performed. Then, 20 ml SniPha 360, diluted in 100 ml 0.9% NaCl were dropwise applied onto the infected para-aortic tissue. Then, two endo-sponges (Endo-SPONGE?, B.Braun, Melsungen, Germay) were placed on the small and large curvature of the aortic arch and the proximal descending aorta respectively, followed by a V.A.C.? GRANFOAM? Dressing sponge (18?12.5?3.2 cm, KCl Medizinprodukte GmbH, Wiesbaden, Germany) (FIG. 2C). The endo-sponges were connected to the V.A.C. VERAFLO? Therapy system (KCl Medizinprodukte GmbH). To avoid contact of the sponges to the lunge a Suprasorb? CNP Drainage film (25?20 cm, Lohman-Rauscher GmbH & Co., Neuwied, Germany) was placed above the sponges. The thorax was closed after placing a chest tube and the patient was refered to intermediate care unit.

[0285] There, once daily, the intrathoracic fluid was pumped out via the V.A.C. VERAFLO? therapy system two hours prior bacteriophage treatment, followed by three times flushing and draining of the sponges with 500 ml 0.9% NaCl, respectively. Afterwards, the endo-sponges were flushed with 20 ml SniPha 360, diluted in 100 ml 0.9% NaCl. Both the endo-sponges drainage and the chest tube were clamped until the next day. FIG. 15, FIG. 16, FIG. 17

[0286] As the second step, the patient was re-thoracotomized after three days. After extraction of all vacuum sponges, the aorta and its surrounding tissue were covered with 40 ml SniPha 360 incorporated in 15.8% hydroxyethylcellulose gel. The thorax was closed and the patient was transfered to intermediate care unit.

[0287] The third step was performed after another three days. Therefore, two sterile RELAY NBS PLUS stent-grafts (Vascutek Terumo-Bolton Medical, Vascutek Germay GmbH, Hamburg, Germany) were released coated with a mixture of 40 ml SniPha 360 and 15.8% hydroxyethylcellulose gel. Afterwards the externally bacteriophage-coated grafts were re-assembled for endovascular placement. This was performed via the left common femoral artery. After overview angiography the two grafts were placed with small overlapping of the infected stent-graft. FIG. 18, FIG. 19

[0288] All invasive procedures were uneventful and no side effects were observed. After the endovascular treatment the patient was referred to a regular ward and recovered soon. Infection parameters decreased, the antibiotical medication was discontinued and the patient recovered. The signs of vasculitis disappeared as well. After four weeks of prolonged physio-therapeutical mobilization in hospital, the patient was discharged to follow-up rehabilitation therapy in good general condition.

[0289] A PET-CT scan performed three months after the bacteriophage treatment did not reveal signs of infection in or around the thoracic aorta were detected. The patient recovered further while infection parameters were undetectable. FIG. 20

Discussion

[0290] This case demonstrates a successful treatment of an infected endovascular stent graft by means of local bacteriophage treatment. To our knowledge, this is the first time a stent-graft was impregnated with bacteriophages for local endovascular application.

[0291] Bacteriophages are known as a potent anti-bacterial treatment due to their lytic activity. Compared to other antibacterial therapeutic strategies like local Rifampicine treatment, bacteriophages have no cytotoxic effects on vascular cells.sup.1. In turn, they have the advantage that they act both on multi-drug resistant bacteria as well as biofilm-organized bacteria. Recently, a case series of eight patients with infections of vascular grafts, surgical wounds or implanted medical devices further demonstrated the feasibility of using different bacteriophages with lytic activity for successful treatment of bacterial infections.sup.2. Although bacteriophages were used for successful treatment of infections of vascular implants, bacteriophage treatment is still not common and no officially recommended option for infections in the Westernized hemisphere.

[0292] In present case, the physical condition and the significant comorbidieties disqualified the patient for a surgical resection of the infected stent-graft and anataomical reconstrunction of the thoracic aorta. By applying bacteriophages both into the vascular lumen as well as onto the peri-prothetic tissues the graft infection with Staphylococcus aureus was successfully treated. The endovascular application of bacteriophages using a releasable stent-graft coated with bacteriophages and re-assembled under sterile conditions before it is insertion into the patient was an important issue of the approach. The intravascular application of phages intravascular directly to the infection site, thus assured a maximum concentration, contact time and invasion of the bacteriophages into the infected tissue.

[0293] Although multiple operative steps, including two times thoracotomy and the endovascular stent graft application, were performed, the respective distress caused by each procedure was markedly less compared to classical surgical treatment. The prolonged postoperative period at the hospital was due to the already initially weak condition of the patient, which required an extensive physiotherapeutical mobilization.

[0294] Since the physical condition of the patient significantly improved over the time and a three month follow-up PET-CT scan revealed no signs of infections, it could be assumed that the bacteriophage treatment was successful. However, there is an ongoing follow- up for the patient to assure a lasting treatment success.

[0295] In summary, this case report demonstrates that bacteriophage treatment could be a curative treatment option for patients that are not suitable for extensive surgical approaches. It is of particular importance that this success was only possible due to the hydrogel comprising HEC and bacteriophages according to the first aspect of the present invention, which allowed localization of phages in situ at the site of infection as well as continuous bacteriophage release in a retarded manner.

EXAMPLE 3

Successful Treatment of a Chronically Infected and Occluded Aorto-Bifemoral Dacron? Bypass with Bacteriophages

Objectives:

[0296] Graft infections are severe and dreaded complications in vascular surgery. The surgical resection of infected aortic grafts is associated with high mortality and morbidity. Therefore, alternatives to inadequate antibiotic treatment and extensive surgery are indispensable.

Case:

[0297] A 66 year-old patient was admitted with an infection of a chronically occluded aorto-bifemoral Dacron? prosthetic bypass. After various transfemoral surgical recanalization attempts in the anamnesis, there were hostile tissue conditions on both femoral sides with chronic wound infection and exposed grafts. Local infection was confirmed by PET-CT imaging. Due to the patient's comorbidities, nothing but the sole explanation of the prosthetic bypass was medically indicated and reasonable. Further we intended to treat the bilateral femoral wound healing disorder. Bacteriophages were contemplated to be an alternative therapy option for intra- and postoperative therapy of the graft related soft tissue infection. After relaparotomy, the infected aortic prosthesis was extirpated, and the aorta was sutured. Bacteriophage suspension was instilled on a Tabotamb-Snow?, which was then placed retroperitoneally. After the femoral anastomoses had been discontinued, a bacteriophage-soaked fleece was placed bilaterally on the femoral side, using the same principle. The wounds were mobilized and closed without further drainage. After 10 days of inpatient stay, the patient could be discharged with subjective well-being, irritation-free wound conditions and without systemic inflammation parameters. PET-CT imaging at three months post intervention did not show signs of infection around the aorta or both femoral regions.

Summary:

[0298] This case demonstrates the supportive antibacterial effect of bacteriophages in septic aortic surgery and the successful secondary closure of chronically infected femoral wounds in high-risk patients. Above all, it demonstrates the superior efficiency of the hydrogel comprising HEC and bacteriophages according to the first aspect of the present invention, which allowed localization of phages in situ at the site of infection as well as continuous bacteriophage release in a retarded manner.

Background

[0299] In vascular surgery, infections of the vascular grafts are considered to be severe complications. Especially infections of aortic grafts are associated with a high morbidity and mortality of up to 75%. Since these procedures are often performed in patients with multiple comorbidities, the required explantation of the infected graft and the extensive struggle with the related abdominal infection is related with an early postoperative morbidity and mortality of even over 20%. Despite the initial achievement of a successful treatment, the general rate of reinfection can be up to 20% of cases. This is mainly due to bacterial colonies embedded in the pen-prosthetic tissue, which then form a surface-adherent biofilm and hence have an up to 1000-fold greater resistance to antibiotic administration. Even a targeted antibiosis appropriate to antimicrobial susceptibility testing can only suppress a graft infection but does not constitute a curative treatment option. The most common pathogenic bacteria associated with graft inflammation are Staphylococcus aureus, Staphylococcus epidermidis and other coagulase-negative staphylococci, Enterobacterales, Pseudomonas aeruginosa and corynebacteria [3]. These bacteria regularly enhance their specific virulence by attaching to the prosthetic material, and hence averting the local immune response by forming biofilms, that hinder phagocytosis. Furthermore, systemic antibiotic therapy is often inadequate due to the lack of effective saturation concentrations within the inflammatory periprosthetic tissue. In order to reduce the morbidity and mortality associated with the often inevitable surgical treatment, less invasive approaches to adequately treat the infection of the surrounding tissue are urgently needed. In this context, bacteriophages and their bacteriolytic activity are a promising therapeutic option.

Case

[0300] In November 2020, a 66 year-old male patient was referred to the emergency ward by his general practitioner with the clinical symptom of an acute abdomen. The examination revealed ubiquitous tenderness on all quadrants with peritonism in the lower abdomen. An infection with SARS-CoV-2 was ruled out. Further examination showed an elevated body temperature of 39.2? C., and blood testing revealed a leukocyte count of 9.4?109/l, as well as an elevated serum C-reactive protein of 90.2 mg/l. The chest X-ray depicted no evidence of pneumonia. An endocarditis was ruled out. Calculated antibiotic therapy with ampicillin/sulbactam was started in the usual dosage intravenously. Blood cultures were positive for Methicillin-susceptible Staphylococcus aureus. Secondary findings included the status of ubiquitous arterial occlusive disease. Due to the necessity of numerous vascular operations on both legs, the patient had eventually undergone a thigh amputation on the right side 12 months earlier; the left side revealed a chronically occluded polytetrafluorethylen (PTFE) Stockmann bypass still in situ.

[0301] After various transfemoral surgical recanalization attempts in the anamnesis, there were hostile tissue conditions bifemoral with a chronic wound infection leading to exposed graft material. Wound swabs exposed the presence of Staphylococcus aureus and Escherichia coli, indicating a polymicrobial infection. The peripheral blood flow of the lower limbs was compensated. Initially, a CT scan of the abdomen was performed, whereupon an occluded and infected aorto-bifemoral graft was assumed. The subsequently performed PET-CT scan displayed a visibly increased metabolic activity in the area of the graft, so that we diagnosed a chronically occluded and infected aorto-bifemoral prosthetic bypass with subsequential bifemoral infections, leading to the cutaneous wound healing disorder. FIG. 21

[0302] Due to the patient's comorbidities, we generally intended an operation and anesthesia time as short as possible with an efficacious treatment by explanting the prosthetic bypass. Further we planned to forego a lavage program for the septic abdomen and intended a primary closure of the abdomen. In order to treat the local inflammation in the abdominal and femoral areas in the long term intra- and postoperatively, the use of bacteriophages was considered to be plausible alternative therapy option in this case. The patient himself favored an alternative solution compared to an indefinite lasting systemical antibacterial treatment. Therefore, an experimental approach using local bacteriophage application was intended as a last resort treatment in line with Article 37 of the Declaration of Helsinki and in unity with the local ethics committee (A 2021-0208).

Bacteriophage Treatment

[0303] As a curative therapeutic strategy an intra and extra abdominal application of SniPha 360 (Phage24.com, Austria) was executed. SniPha 360 is a commercially available bacteriophage cocktail of lytic bacteriophages against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Streptococcus pyogenes, Proteus vulgaris and Proteus mirabilis. After outlining the potential risks but also benefits of the experimental procedure, the patient consented to the therapy. When performing the relaparotomy, cloudy fluid appeared within the abdomen. After an initial lavage, the retroperitoneum was opened, and the proximal aorta was prepared for clamping. The aorto-bifemoral Dacron? prosthesis presented a shell of a biofilm and was embedded in putrid fluid. The infected aortic prosthesis was extirpated, and the aorta was then sutured over. The prosthesis was retrieved femorally after mobilization of the legs of the prosthesis. The bacteriophage suspension was instilled on Tabotamb-Snow?, which was placed retroperitoneally around the infection. The retroperitoneum and abdomen were primarily closed without further drainage. After removing the femoral anastomoses, the wound conditions were debrided, mobilized and lavaged with a sharp spoon. A bacteriophage-soaked fleece was then placed bilaterally on the femoral side by the same principle, and the wounds were closed again without further drainage.

[0304] The operation time was 52 minutes, without significant blood loss. Subsequently the patient could be taken to the intensive care unit and extubated without the need for catecholamines. After 10 days of hospitalization, the patient could be discharged with subjective well-being, irritation-free wound conditions and normal findings for inflammatory values in the blood. PET-CT imaging at three months post intervention did not show signs of infection enclosing the aorta or both femoral regions.

Discussion

[0305] This case demonstrates a successful treatment of a chronically infected occluded aorto-bifemoral Dacron? bypass by a local bacteriophage application. Especially, it was demonstrated that this success was only possible due to the hydrogel comprising HEC and bacteriophages according to the first aspect of the present invention, which allowed localization of phages in situ at the site of infection as well as continuous bacteriophage release in a retarded manner.

[0306] It is assumed that around 50-65% of prosthesis infections are a result of bacterial contamination during surgery [3,4]. A general distinction is made between early (up to 30 days postoperatively) and late infections, although the classification is arbitrary [3,4]. Early prosthesis infections are often assumed to be a consequence of intraoperative contamination and late infections to be a result of hematogenous bacterial spread, but profound evidence for this is limited. Late infections are usually caused by insufficient tissue integration of the prosthesis into the graft bed. Common pathogenic agents are staphylococci, enterobacteria and corynebacteria [3,4]. Bacteriophages (or simply phages, Greek: bacteria eater) are viruses that selectively infect bacterial cells and were first described in 1917 by the Canadian Felix Hubert dHerelle.

[0307] Currently Bacteriophages are known as a potent anti-bacterial treatment due to their lytic activity. They are considerably stable when exposed to the inflammatory environment and contribute significantly to the regulation of global bacterial mass. A bacteriophage can only multiply where its host is. They are highly specific and therefore predominantly affect strains within one bacterial species, rarely crossing species boundaries [5].

[0308] In the first (lytic) cycle of viral reproduction, phages kill their corresponding bacteria through lysis: once infected, the bacterium host cell then starts the process of reproduction, the destruction of the bacterium, and the release of new phage particles; this process is controlled by enzymes and an interaction of bacterial and phage genes. In the second (lysogenic) cycle, the bacteriophage nucleic acid is integrated into the host bacterium's genome or forms a circular replicon in the bacterial cytoplasm. Compared to other antibacterial therapeutic strategies like local Rifampicine treatment, no cytotoxic effects on vascular cells could be found for bacteriophages.

[0309] In addition, they are effective on multi-drug resistant bacteria as well as biofilm-organized bacteria. Recently, in a case series of eight patients with infections of vascular grafts, surgical wounds or implanted medical devices further demonstrated the feasibility of using different bacteriophages with lytic activity for successful treatment of bacterial infections. Although bacteriophages were used for successful treatment of infections of vascular implants, bacteriophage treatment is still not common and not an officially recommended option for infections in the westernized hemisphere. The retro- and intraabdominal application of phages directly to the infection site ensured a maximum concentration, contact time and invasion of the bacteriophages into the infected peri graft tissue. We were able to perform a short operation time, a definite treatment in respect to complete skin/wound closure and the forego of any drainages. No bacteriophage related clinical adverse events had been detected in our case. A three-month follow-up PET-CT scan revealed no signs of infections. It could be assumed that the bacteriophage treatment was successful.

[0310] In order to treat the local inflammation in the abdominal and femoral areas in the long term intra- and postoperatively, we perceived the use of bacteriophages as an alternative therapy option in antibacterial local therapy. However, there is an ongoing follow-up for the patient to assure a lasting treatment success. In summary, this case report demonstrates that bacteriophage treatment could be a curative treatment option for patients with bacterial graft- and pen graft infections that are not suitable for extensive surgical approaches.

EXAMPLE 4

Testing Bacteriophages Activity in Lyophilizate

Methods

[0311] In order to test the activity of bacteriophages in lyophilizated hydrogel, five lyophilizates from phage gel (composition: HEC: 13 g=13%, CaCl.sub.2-Solution: 43 g=43%, glycerol to 85%: 27 g=27%, water: 17 g=17%) were prepared (see FIG. 25). Subsequently, the lyophilizated hydrogels were centered on an agar-agar plate set with Staphylococcus aureus (see FIG. 26) and incubated at 36? C. for 24 h.

Results

[0312] The freeze-dryed hydrogel was shown to be degraded via the gel state and then diluted (here: mainly by water from the culture medium). The activity of the phages remained, which was recognizable by the corresponding bacteria-free (circled) plaques on the culture medium (see FIG. 27).

EXAMPLE 5

Testing Phage Release Out of Lyophlizated Hydrogels

Methods

Preparation of Lyophilizates

[0313] Hydrogels B and C used for lyophilization have the following composition: [0314] HEC: B=7 g=7%/C14 g=14% [0315] CaCl2-Solution: 43 g=43% [0316] Glycerol 85%: 27 g=27% [0317] Water: B=10 g=23%/C=16 g=16%

[0318] These hydrogels comprising bacteriophages were prepared as sterile gels and lyophilization was performed in a sterile environment as well.

[0319] The following lyophilizated products were prepared and tested as described below: [0320] B1 7 g Gel+3 ml BPh-Buffer*+4 ml Aqua ad inj..fwdarw.>15?10.sup.11 PFU/ml [0321] B2 7 g Gel+6 ml BPh-Buffer*+1 ml Aqua ad inj..fwdarw.>30?10.sup.11 PFU/ml [0322] C1 7 g Gel+3 ml BPh-Buffer*+4 ml Aqua ad inj..fwdarw.>15?10.sup.11 PFU/ml [0323] C2 7 g Gel+6 ml BPh-Buffer*+1 ml Aqua ad inj..fwdarw.>30?10.sup.11 PFU/ml

*BPh-Buffer>5?10.SUP.11 .PFU/ml

[0324] Bph-Buffer: Tris buffer comprising sodium chloride, magnesium chloride (?7 H2O) and Tris-HCl, pH=7.4

[0325] Of the products B1, B2, C1 and C2, C1 and C2 are the most solid formulation due to the gel former content (double amount of HEC), whereby Variant 2 of B and C (B2 and C2) contains the double concentration of BPh.

Release Tests

[0326] First, the lyophillizated products B1, B2, C1 and C2 were each released in 100 ml of sterile, physiological NaCl solution (0.9%) over 2 h. Thereby, NaCl solution was used, which was previously sterilized by sterile filtration. Further used utensils, such as bottles, stirring fish, etc., were sterilized by prior via steam sterilization.

[0327] Over the next 2 hours, samples were drawn by extracting 1 ml every 15 min, whereby the sample volume was not replaced. If necessary, a sample was diluted. Subsequently, samples were distributed on set Staphylococcus aureus plates and incubated for 24 h at 37? C. In total, 2 runs per gel variant were performed (n=2).

Results Release Tests

[0328] To sum up, the results showed that there is a strongly retarded release of phages from freeze-dryed hydrogels (see FIG. 29).

[0329] Moreover, the curves show that a higher proportion of gel former (C1 and C2) shows stronger retarded release in comparison to a lower proportion of gel former (B1 and B2).

[0330] Further, a lower phage conc. (pfu/ml) in the starting gel (B1, 01) consequently also showed a lower phage release per time in comparison to a higher phage concentration (B2, C2) in the starting gel.

EXAMPLE 6

Therapy of Acne Inversa Using a Bacteriophage Cocktail in Connection with a Galenic Carrier in a Clinical Comparison to the Gold Standard

Abstract

[0331] Acne inversa is a chronic skin disease. Painful inflammation develops in the area of the hair follicles. As a result, abscesses, fistulas and nodular scarring can develop. The inflammation occurs mainly in the armpits and in the groin, anal and genital regions. In the present treatment attempt, findings in the left axilla were applied in accordance with a treatment attempt according to ? 37 of the Helsinki Declaration with a hydrogel comprising HEC and bacteriophages, while a clinically similar finding on the right gluteal side was treated conventionally with open wound treatment.

[0332] In the short and long term, there are clear clinical advantages with regard to bacteriophage therapy.

Introduction

[0333] The patient was presented with the referral of the family doctor with suspected acne inversa at several locations, especially left axillary and right gluteal (Hurley stage II/III). The patient had already had an axillary operation in 1997 and a posterior operation on the thighs in 2011 due to acne inversa.

[0334] Since last year there has been a continuous deterioration under drug therapy with adalimub (Hyrimoz) 40 mg and cefpodoxime 200 mg and local Fucidine. The patient was in severe pain and could hardly sit, right arm rotation was painful and restricted movement. Intermittent fever was mentioned. Associated diseases are arterial hypertension, a factor V Leiden mutation, the Z.n. Pulmonary artery embolism in 1996, 1998, 2003 and nicotine abuse.

[0335] Findings on inpatient admissionin the axillary, inguinal and, above all, the gluteal area on the right, therewere inflammatory nodules that were tender to pressure, furthermore abscesses, fistula and scar formation, equivalent to Hurley stage II/III (see FIG. 31). In the laboratory blood there was a leucotytosis with WBC 21?10 high 9/l and a CRP of 30 mg/l (3 mg/dl). Wound swabs were not taken.

Methods

[0336] Admission was initiated for surgical care and in connection with planned bacteriophage injection as a healing attempt according to ? 37 Helsinki Declaration. A local anaesthesia was performed with 20 ml Scandicain 1% subcutaneously in the aera of surgical axillary access (see FIG. 31, top left). After en-bloc resection via two separate accesses to the infected soft tissue, the wound surface was injected subcutaneously with 20 ml of a bacteriophage galenic in a viscous state (see FIG. 31, top right and bottom left) comprising phage cocktail SniPha 360 from the company Phage 24? with a phage concentration of at least 1?10.sup.5 against the germs S. aureus, Streptococcus pyogenes, E. coli, P. aeroginosa, Proteus vulgaris and Proteus smirabilis (composition of galenic: HEC: 13 g=13%, CaCl.sub.2-Solution: 43 g=43%, glycerol 85%: 27 g=27%, water: 17 g=17%). The skin was then mobilized and primarily closed without further drainage (see FIG. 31, bottom rigth). In the course of the inpatient treatment, only dry dressings were changed. The sutures were removed 12 days post OR.

[0337] In contrast to this, general anaesthesia needed to be performed because of persisting pain under local anaesthesia. In this topic, open excision and open wound treatment were chosen as the gold standard therapy for acne inverse on the right gluteal side. The introperatively adapted VAC pump was checked regularly and could be removed after 5 days. The wound was showered daily afterwards and was clean and free of irritation before discharge. The further procedure was daily cleaning with Octenisept solution and douching of the wound as well as a moist wound dressing until the wound had completely granulated

Results

[0338] The patient presented to the clinic 2 weeks and 10 weeks after the surgical intervention for clinical follow-up. The right axillary wound was continuously clean and dry with a 1 mm large, clearly exuding pore in the middle of the larger access wound (see FIG. 32, left), which was closed without irritation 10 weeks after the operation (see FIG. 32, right). In the first wound check after 2 weeks, the gluteal wound was granulating but covered with fibrin (see FIG. 33, top). With continued wound treatment, a scarred, granulating wound was established 10 weeks after the operation (see FIG. 33, bottom).

Discussion

[0339] Acne inverse is a painful, chronic inflammatory skin condition that primarily affects the armpits, groin, pubic area and anus. The disease often begins with hair root inflammation and then spreads in the form of recurring inflammation and abscesses. An estimated 1% of the population is affected. A large number of bacteria can be found in acne inversa/hidradenitis suppurativa lesions, in particular Staphylococcus aureus. The disease is often diagnosed too late and at an advanced stage. Those affected often withdraw out of fear and shame, which can disrupt their professional career, personal and social relationships and lead to depression.

[0340] Depending on the severity, divided into Hurley grades Ito III, those affected suffer from recurring pus the weeping wounds. Individual inflammatory nodules or abscesses in surrounding healthy tissue are usually found in patients classified as Hurley grade I. In grade II, progressive, defined inflammation with scarring and fistula formation is described. In grade III, there are extensive, interconnected abscesses and fistula tracts. [0341] Hurley I: Local or systemic administration of antibiotics, if necessary surgical removal of individual lesions injuries/areas [0342] Hurley II: Systemic administration of antibiotics, administration of antibodies, surgical removal of individual injuries, if necessary removal of superficial tissue layers using a laser [0343] Hurley III: Systemic antibiotics, administration of antibodies, radical surgical removal of the affected tissue

[0344] For wound treatment after an operation in Hurley grade according to the guideline therapy, it is recommended not to sew up the wound, but to let it heal openly. Suitable wound dressings and, if necessary, negative pressure wound therapy (NPVVT) are used to cover the open wound.

[0345] The present example impressively showed the potency of bacteriophage application in direct comparison to conventional treatment methods. Both the early inpatient and the postoperative course were unremarkable in relation to the axilla treated with bacteriophages, while in the area of the gluteal wound a complex, lengthy and cosmetically poor healing process could be documented.

[0346] The success of using the bacteriophage cocktail without prior sensitivity testing as part of a phagogram could be attributed to the use of different phages. The use of several bacteriophage increased the sensitivity rate and also targeted mixed infections. The subcutaneous application of standardized bacteriophage solution in connection with a carrier increased the topical residence time and the local bacteriophage concentration in the initial phase of infection treatment. A gel galenic was used as an application medium in addition to the bacteriophage solution in order to prevent the bacteriophage solution from running off the targeted area quickly. In this respect, the described gel galenics act like a reservoir for the phages. The application of a liquid solution is considered to be less effective, since the bacteriophage concentration cannot be optimally maintained topically.

[0347] The bacteriophage application in form of a hydrogel according to the present invention has proven to be a patient-friendly, inexpensive, side effect-free and fast therapy approach with excellent results in the present treatment trial. From a medical economic point of view, advantages for the bacteriophage application can be seen due to the clearly different healing processes.

Summary

[0348] In the present case report, the application of a bacteriophage cocktail with a galenically defined carrier, which together form of a hydrogel according to the present invention, is superior to the conventional treatment of acne inverse type II/III according to Hurley.

EXAMPLE 7

Comparison of Wound Healing of Wounds Caused by Subcutaneous Bacterial Infection in Mice Treated with Various Forms of Bacteriophage-Containing Hydrogel

Introduction

[0349] Subcutaneous injection of Staphylococcus aureus in healthy mice generally leads to a bacterial infection causing open wounds. The reduction of bacterial burden is hence mandatory for a healing of the wounds as bacterial infection cause and expand skin destruction. Especially, wounds usually close faster when less bacteria are present. In the course of the infection, healing of these wounds supported by treatment with a hydrogel according to the present invention leads to wound seize reduction until upon complete healing, the wounds are entirely closed.

[0350] Consequently, wound seize reduction is an indirect indication for the effect of the respective treatment. The time, and hence the trend of how fast the wounds reduce over the time is an indirect but solid scientific read out for the used mice model.

Description:

[0351] In a mice model 5 groups of mice with 22 mice per group were tested. On day one all mice have been infected subcutaneously with the same amount of Staph. Aureus. Therefore, 100 ?L of bacterial suspension containing an appropriate number of colony forming units (CFU) was injected subcutaneously into the shaved area under ketamine/xylazine anaesthesia.

[0352] On day 3 all mice showed wounds that were treated with:

TABLE-US-00003 I HEC in the composition described n.a. 0.5 ml/mouse II Phage-Solution 10.sup.5 pfu/ml 0.5 ml/mouse III Phage-Solution + HEC in the 10.sup.5 pfu/ml 1.0 ml/mouse composition described 1:1 IV Phage-Solution + HEC in the 10.sup.2.5 pfu/ml 1.0 ml/mouse composition described 1:2 V non treatment n.a. (HEC composition: HEC (Hydroxy-ethyl-cellulose): 13 g = 13%, CaCl.sub.2-Solution*: 43 g = 43%, glycerol 85%: 27 g = 27%, water: 17 g = 17%)

[0353] Thereby, the phage-solution used is SniPha 360 PhagesPhage Solution, Sanubiom.

[0354] The formulation for groups III and IV was prepared as follows: adequate volume of the HEC in the composition described was placed in a first Omnifix Luer lock syringe, while a second Omnifix syringe was filled with the phage solution. The two syringes were connected with an Omnifix adapter and the phage solution was pushed in the carrier. The to formulation was fully mixed by the pushing of the solution back and forth between two syringes through the connector at least ten times.

[0355] On the following days, the respective wound seizes were measured (based on length and width of each lesion), averaged and trended. For ratio evaluation, the slope of the phage solution group was taken as the comparison group so that the slope ratio=1. Test results have been considered up to day 10, because afterwards the immune system overlapped the healing effects of the respective products.

Results:

[0356] The results show a superiority of the gel-phage combinations:

TABLE-US-00004 line slope Slope ratio I ?0.1145 1.5226 HEC in the composition described II ?0.0752 1.0000 Phage-Solution III ?0.1628 2.1649 Phage-Solution + HEC- Composition 1:1 IV ?0.1845 2.4535 Phage-Solution + HEC- Composition 1:2 V ?0.0796 1.0585 non treatment

[0357] This is particularly evident from group IV, which has the best overall slope and a 2.5 times better slope in trending compared to Group II. Although, it holds only half the phage concentration in comparison to Groups II and III. Hence, Group I is 1.5 times better and Group II is about 2 times better concerning the trend of wound seize reduction. The Group II is comparable with Group V, that was left untreated.

[0358] The previously described trending shows the superiority of the phage-gel combinations over the non-treatment group and the phage-solution group (Group II).

[0359] Many products are used for wound treatment, but not a HEC gel in the composition described. The test showed that HEC in the composition described not only adequately carried the phages at the site of application, adhered to it adhesively and released the phages in a correspondingly retarded manner. In addition, it was also beneficial to wound healing: the HEC gel alone, in the composition described, without phages (Group I) reduced the wound area in the trending 1.5 times faster than the phage solution. This effect can be explained on the one hand by the water contained and the hydrophilic gel properties. In addition, the adhesive character of the HEC in the composition described here is also evident: due to the tissue-friendly composition, the wound moistened by the hydrogel healed better than the wounds of the mice in the phage solution group, also due to the physical shielding to the outside.

[0360] In Group II, the phage solution quickly ran off the wounds when it was applied to them. Even a covering with the appropriate wound covering could not prevent this or increase the probability of a phage-bacterium interaction. This is clearly shown by the comparable values of the phage solution group (Group II) and the non-treatment group (Group V).

[0361] Groups III and IV showed two to two and a half times the wound reduction rate compared to Group II (phage solution). Particularly noteworthy is Group IV, which carried only half the phage concentration compared to Groups II and III. The properties of the HEC in the described composition are most evident here. Due to the properties already explained, wound healing was accelerated. The continued release of phage increased the interaction of phage and bacterium.

[0362] The phage solution (Group II) and Group III were carried out with the same phage solution quantity, here only the difference in connection with the carrier became apparent: Group III was better (=faster) by more than double with regard to wound healing. Further, it was shown that the more the carrier is increased in the proportion, the more the retarding release is forced: Group IV showed the fastest wound healing rate in trending with a phage concentration of only 10.sup.2.5 pfu/ml.

[0363] As a result, with the HEC described in this composition, therapeutic success was shown with phage concentrations of 10.sup.5 pfu/ml (Group III) only, which was 2-fold superior to the phage solution (Group II).

REFERENCES TO EXAMPLE 2

[0364] 1. Szilagyi DE, Smith RF, Elliott JP, Vrandecic MP (1972) Infection in arterial reconstruction with synthetic grafts. Ann Surg 176: 321-333. [0365] 2. {umlaut over (Z)}uhlke HV, Harnoss BM, Lorenz EP (1994) Postoperative Ilnfektionen in der Gef??chirurgie. In: Septische Gef??chirurgie Blackwell Wiss Verlag.

REFERENCES TO EXAMPLE 3

[0366] [3] Kirklin JK, Pagani FD, Kormos RL, Stevenson LW, Blume ED, Myers SL, et al.

[0367] Eighth annual INTERMACS report: Special focus on framing the impact of adverse events. The Journal of Heart and Lung Transplantation 2017;36:1080-6. [0368] [4] Kim J, Feller ED, Chen W, Liang Y, Dilsizian V. FDG PET/CT for Early Detection and Localization of Left Ventricular Assist Device Infection: Impact on Patient

[0369] Management and Outcome. JACC Cardiovasc Imaging 2019;12:722-9. [0370] [5] Baddour LM, Wilson WR, Bayer AS, Fowler VG, Tleyjeh IM, Rybak MJ, et al. Infective Endocarditis in Adults: Diagnosis, Antimicrobial Therapy, and Management of Complications: A Scientific Statement for Healthcare Professionals From the American Heart Association. Circulation 2015;132:1435-86.

REFERENCES TO EXAMPLE 7

[0371] 6F. Altamirano , J. BarrPhage Therapy in the Postantibiotic Era-Clin Microbiol Rev. 2019 Jan 16;32(2):e00066-18. doi: 10.1128/CMR.00066-18. [0372] 7D. Malik , I. Sokolov , G. Vinner , F.o Mancuso , A KirpichnikovaFormulation, stabilisation and encapsulation of bacteriophage for phage therapy. Adv Colloid Interface Sci. 2017 Nov;249:100-133. doi: 10.1016/j.cis.2017.05.014. Epub 2017 May 14. [0373] 8L. Kasman, J. NorrisOvercoming the Phage Replication Threshold: a Mathematical Model with Implications for Phage TherapyJournal of Virology 2002 Vol. 76, No. 11, doi.ord/10.1128/ivi.76.11.5557-5564.2002 [0374] 9E. Morello, L. DebarbieuxPulmonary Bacteriophage Therapy on Pseudomonas aeruginosa Cystic Fibrosis Strains: First Steps Towards Treatment and Prevention2011 plos on collection psychiology, doi.org/10.1371/joumal.pone.0016963 [0375] 10H. madavi, S. padmanabhanTherapeutic Potential of Staphylococcal Bacteriophages for Nasal Decolonization of Staphylococcus aureus in MiceAdvances in Microbiology Vol.3 No.1(2013), Article ID:29179,9 pages DOI:10.4236/aim.2013.31008 [0376] 11D. Rhoads, A. SulakvelidzeBacteriophage therapy of venous leg ulcers in humans: results of a phase I safety trialJournal of wound care 2013, Vol.18, No.6, doi.org/10.12968/jowc.2009.18.6.42801