USE OF ADVANCED PLATELET-RICH FIBRIN IN PREPARING MEDICAMENT FOR TREATMENT OF DIABETIC FOOT ULCER
20230201314 · 2023-06-29
Inventors
- Di ZHU (Beijing, CN)
- Caizhe YANG (Beijing, CN)
- Nan SU (Beijing, CN)
- Hongmei CHEN (Beijing, CN)
- Li Xiao (Beijing, CN)
- Ying Chen (Beijing, CN)
- Liangchen WANG (Beijing, CN)
- Chenrui WANG (Beijing, CN)
- Xiaotian ZHANG (Beijing, CN)
Cpc classification
A61K2035/124
HUMAN NECESSITIES
A61P17/02
HUMAN NECESSITIES
International classification
A61P17/02
HUMAN NECESSITIES
Abstract
The present disclosure relates to the technical field of biomedicine, in particular to use of advanced platelet-rich fibrin (A-PRF) in preparing a medicament for the treatment of diabetic foot ulcer. The A-PRF provided by the present disclosure has a loose reticular fibrin structure, can be rich in more platelets and leukocytes, can release a plurality of growth factors and cytokines more persistently, and is more beneficial to tissue regeneration and wound repair. The medicament prepared from the A-PRF shortens the healing period of the diabetic foot ulcer, improves the healing rate, and has an excellent treatment effect and high safety.
Claims
1. A method for treating diabetic foot ulcer, the method comprising using advanced platelet rich fibrin (A-PRF), wherein the A-PRF is prepared according to the following steps: centrifuging blood at 1,500 rpm for 14 minutes, and separating an intermediate gel layer as the A-PRF, wherein the blood is autologous blood collected within 1 minute.
2. A medicament for the treatment of diabetic foot ulcer, wherein the medicament comprises A-PRF and pharmaceutically acceptable excipients.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF THE EMBODIMENTS
[0030] The present disclosure provides use of A-PRF in preparing a medicament for the treatment of diabetic foot ulcer.
[0031] The A-PRF provided by the present disclosure has a loose reticular fibrin structure, can be rich in more platelets and leukocytes, can release a plurality of growth factors and cytokines more persistently, and is more beneficial to tissue regeneration and wound repair. The medicament prepared from the A-PRF shortens the healing period of the diabetic foot ulcer, improves the healing rate, and has an excellent treatment effect and high safety.
[0032] The present disclosure further provides a medicament for the treatment of diabetic foot ulcer, and the medicament includes A-PRF and pharmaceutically acceptable excipients. In the present disclosure, the A-PRF may preferably include A-PRF prepared from autologous blood.
[0033] The present disclosure preferably further provides a preparation method of the foregoing A-PRF, including the following steps: centrifuging the blood at 1,500 rpm for 14 min, and separating an intermediate gel layer as the A-PRF. In the present disclosure, the blood may preferably include autologous blood; more preferably, the blood may include autologous blood collected within 1 min. The present disclosure uses the autologous blood to prepare the A-PRF, which can avoid immune rejection of foreign blood, with high safety.
[0034] To further describe the present disclosure, the use of A-PRF in preparing a medicament for the treatment of diabetic foot ulcer provided by the present disclosure will be described below in detail with reference to examples, but they may not be construed as limiting the protection scope of the present disclosure.
Example 1
[0035] The A-PRF was prepared according to the following steps:
[0036] in strict accordance with aseptic operation, 5 mL of venous blood was placed in an anticoagulant-free vacuum glass tube, shaken well, and put in a balanced centrifuge immediately (within 1 min after blood collection); the tube was centrifuged at 1,500 rpm for 14 min at room temperature and left to stand, the blood samples were divided into three layers, the supernatant was discarded, the bottom red blood cell debris was removed, and the intermediate gel layer was collected to obtain the A-PRF.
[0037] The prepared A-PRF was left to stand in a dry and sterile bending tray, and placed between two sterile gauze layers to squeeze, namely, an A-PRF film was made, which was evenly spread or packed on the wound surface of the diabetic foot; the surface was covered with a sterile gauze impregnated with 1% ethacridine, and the outer layer was dressed with sterile gauzes.
Application Example 1
[0038] A-PRF was prepared from part of the blood from 30 patients with diabetic foot ulcer according to the method of Example 1, and the prepared A-PRF films were applied to the wounds of the 30 patients with diabetic foot ulcer according to the method of Example 1. The wounds were checked once every 2-3 days, and the A-PRF films were changed every 10 days.
[0039] Typical cases were as follows:
[0040] Case 1:
[0041] A 72-year-old female patient with chronic wound of diabetic foot (Wagner grade 3) was admitted to a hospital because of hyperglycemia for 20 years and bilateral foot ulceration for two years. The wound was treated with vacuum-assisted closure therapy and the above A-PRF successively, and photographed on Nov. 30, 2020 (
[0042] Case 2:
[0043] A 93-year-old female patient with chronic wound of diabetic foot (Wagner grade 2) was admitted to a hospital because of hyperglycemia for 18 years and left pretibial skin ulceration for a month. The wounds were treated with the above A-PRF, and the photos were taken on Sep. 1, 2020 (
[0044] Case 3:
[0045] A 65-year-old medium-elderly male with chronic wound of diabetic foot (Wagner grade 3) was admitted to a hospital because of hyperglycemia for 30 years and bilateral foot ulceration for one year. The left foot wound was treated with A-PRF, and the photos were taken on May 8, 2021 (
[0046] Case 4:
[0047] A 70-year-old senile male with chronic wound of diabetic foot (Wagner grade 2) was admitted to a hospital because of hyperglycemia for more than 10 years and left foot ulceration for one month. The left foot wound was treated with A-PRF, and the photos were taken on Sep. 13, 2021 (
Comparative Example 1
[0048] L-PRF was prepared from part of the blood of 30 patients with diabetic foot ulcer and similar conditions as in Application Example 1, and the prepared L-PRF was left to stand in a dry and sterile bending tray, and placed between two sterile gauze layers to squeeze, namely, an A-PRF film was made, which was evenly spread or packed on the wound surface of the 30 patients with diabetic foot; the surface was covered with a sterile gauze impregnated with 1% ethacridine, and the outer layer was dressed with sterile gauzes. The wounds were checked once every 2-3 days, and the L-PRF films were changed every 7 days.
[0049] The L-PRF was prepared according to the following steps:
[0050] in strict accordance with aseptic operation, 5 mL of venous blood was placed in an anticoagulant-free vacuum glass tube, shaken well, and put in a balanced centrifuge immediately (within 1 min after blood collection); the tube was centrifuged at 3,000 rpm for 10 min at room temperature and left to stand, the blood samples were divided into three layers, the supernatant was discarded, the bottom red blood cell debris was removed, and the intermediate gel layer was collected to obtain the L-PRF.
[0051] Typical cases were as follows:
[0052] Case 5:
[0053] A 76-year-old senile female with chronic wound of diabetic foot (Wagner grade 3) was admitted to a hospital because of hyperglycemia for more than 20 years and left foot ulceration for two months. The left foot wound was treated with L-PRF, and the photos were taken on Aug. 21, 2020 (
[0054] Case 6:
[0055] A 72-year-old senile male with chronic wound of diabetic foot (Wagner grade 2) was admitted to a hospital because of hyperglycemia for more than 13 years and left lateral malleolus ulceration for two months. The wound was treated with L-PRF, and the photos were taken on Sep. 28, 2020 (
[0056] The treatment effects of a total of 60 patients in Application Example 1 and Comparative Example 1 were observed and summarized. The results are shown in Table 1 and
TABLE-US-00001 TABLE 1 Treatment effects of different patients Wound healing Median healing period (upper Group rate (%) and lower quartiles) (day) Application Example 1 93.4% 24 (11-52) Comparative Example 1 .sup. 70% 52 (28-74) NOTE: The wound healing rate in Table 1 = the number of healed patients/30 × 100%; since the healing period does not conform to the normal distribution, it is expressed by the median healing period (upper and lower quartiles), and the median healing period = the median of healing period.
[0057] As seen from Table 1 and
[0058] In conclusion, the medicament prepared from the A-PRF provided by the present disclosure shortens the healing period of the diabetic foot ulcer, improves the healing rate, and has an excellent treatment effect and high safety.
[0059] Although the present disclosure has been set forth as above in preferred examples, they are not intended to limit the present disclosure. Those skilled in the art can make various alterations and modifications without departing from the spirit and scope of the present disclosure. Therefore, the protection scope of the present disclosure should be subject to the protection scope defined by the claims.