THYROID MANUFACTURING PROCESS AND SPECIFICATIONS

Abstract

The invention relates to a thyroid manufacturing process, and more particularly, to a novel thyroid manufacturing process which encompasses a new drying step during the thyroid extraction step and a further homogenization, which allow in a thyroid product with a controlled value of hormones, and it is essentially free of virus and bacteria.

Claims

1. A thyroid manufacturing process from porcine thyroid glands, characterized in that it comprises the following steps: i. Mincing of the porcine thyroid glands; ii. Obtention of the thyroid extract, wherein the mincing porcine thyroid glands from step i) are washed by multiple cycles in acetone, filtered and further dried at a temperature that ranges between 80° C. and 95° C., during at least 6 hours, and finally milled; iii. Homogenization of the milled product from step ii) with an excipient to dilute the hormones.

2. The thyroid manufacturing process according to claim 1, wherein the temperature in step ii) is between 85 and 90° C.

3. The thyroid manufacturing process according to claim 1, wherein the excipient in step iii) is selected from lactose, maltodextrin, xylitol, lactitol, and mannitol.

4. The thyroid manufacturing process according to claim 3, wherein the excipient is lactose.

5. A thyroid product, characterised in that no virus nor bacteria is detected, the T4/T3 value is between 4.0 and 4.6, and in that is manufactured from porcine thyroid glands following the process which comprises the following steps: i. Mincing of the porcine thyroid glands; ii. Obtention of the thyroid extract, wherein the mincing porcine thyroids grands from step i) are washed by multiple cycles in acetone, filtered and further dried at a temperature that ranges between 80° C. and 95° C., during at least 6 hours, and finally milled; iii. Homogenization of the milled product from step ii) with an excipient to dilute the hormones.

Description

DESCRIPTION OF THE DRAWINGS

[0017] FIG. 1. Scheme of the obtention of the thyroid extract (step ii)

EXAMPLES

Example 1. Thyroid Manufacturing Process from Porcine Thyroid Glands

[0018] Following the protocol disclosed in United States Pharmacopeia (2022). USP Monograph, Thyroid. USP-NF. Rockville, MD: United States Pharmacopeia, Thyroid is cleaned, dried, and powdered into thyroid gland, previously deprived of connective tissue and fat. It is obtained from domesticated animals that are used for food by humans.

[0019] On hydrolysis it yields not less than 90.0% and not more than 110.0% each of the labeled amounts of levothyroxine (T4) (C.sub.15H.sub.11I.sub.4NO.sub.4) and liothyronine (T3) (C.sub.15H.sub.12I.sub.3NO.sub.4), calculated on the dried basis. It is free from iodine in inorganic or any form of combination other than that peculiar to the thyroid gland. It may contain a suitable diluent such as lactose, sodium chloride, starch, sucrose, or dextrose.

[0020] The preparation process starts when the pig thyroid glands (100 g) are chopped, and 10 volumes of acetone are added and stirred for at least 1 hour at 25° C. Then, the previous mixture is decanted for 1 hour, and the supernatant is siphoned (this process is repeated three times).

[0021] Then, the product is filtered a with paper filter with vacuum and dried with vacuum between 85 to 95° C. during at least 6 hours; the product is weighed. Subsequently, the product is placed in the mill, the product is sieved with a 500-micron sieve and the samples are sent in 20 mL vials to determine the activity T4/T3. This “final” product is then mixed with lactose to meet market requirements for Thyroid content.

Example 2. Specification for the Final Product

[0022] Appearance is performed by visual inspection of the product, describing color.

TABLE-US-00001 Parameter Limit Appearance Low-density, pale brown powder Identification The retention times of the peaks for liothyronine and levothyroxine of the Sample solution correspond to those of the Standard solution, as obtained in the Assay. Limit of inorganic iodides Not more than 0.01% Loss on drying Not more than 6.0% Total aerobic count Not more than 10.sup.3 ufc/g Total yeasts and moulds count Not more than 10.sup.2 ufc/g E. coli Absence/g Salmonella Absence/10 g Acetone Not more than 5000 ppm Fat Not more than 4.0% Residue on ignition Not more than 5.0% Assay Liothyronine (T3, odb) 24.3-29.7 μg/grain Levothyroxine (T4, odb) 103-125 μg/grain T4/T3 ratio 4.0-4.6

[0023] Identification, Limit of inorganic iodides, loss on drying, and assay of T3 and T4 are performed as described in USP Thyroid monograph. T4/13 ratio is obtained by calculation using T4 and T3 values.

[0024] Microbiological tests (Total aerobic count, Total yeasts and moulds count, Salmonella and E. Coli) are analyzed as described in USP 61, Microbial Enumeration Tests, and USP 62, Tests for Specified Microorganisms.

[0025] Fat content is determined as described in USP Pancrelipase Monograph, Fat.

[0026] Residue on ignition is determined as described in USP 281, Residue on ignition. Acetone is determined by Gas Chromatography with Flame Ionization Detection.

Example 3. Evaluation of the Presence of Porcine Circovirus Type 1 (PCV-1) Infectious Viral Particles on PK15 G6 Cells by Infectious Real-Time Qualitative PCR of PCV-1 Spliced mRNA Sequence

[0027] DNA sequence for PCV-1 were identified within the tested sample. Purpose was to determine if PCV-1 viral infectious particles were still present in the sample tested.

[0028] Tests performed in accordance with Standard Operating Procedures (SOP) TE1088 version 13, TE2041 version 10 and TE1128 version 2.

[0029] In the in vitro assay in cell culture, no infectious particles of PCV-1 were detected.

Example 4. Evaluation of the Presence of Porcine Circo Virus Type 2 (PCV-2) Infectious Viral Particles on PK 15 Cells

[0030] DNA sequence for PCV-2 were identified within the tested sample. Purpose was to determine if PCV-2 viral infectious particles were still present in the samples tested.

[0031] PCV-2 Quantitation by PCR

[0032] Positive with Ct at 33.2 12946 genomic copy/mL

[0033] PCV-2 Virus Strain Identification by Sequencing of ORF-2 Gene

[0034] Result negative: no full genomic sequences can be obtained

[0035] PCV-2 Virus Isolation on PK15 Cells

[0036] Result negative

[0037] PCV-2 Virus Titration on PK15 Cells

[0038] Result negative

[0039] Samples Tested in triplicate were titrated in PK 15 cells for PCV2. It turned out that no detectable titre could be determined.

[0040] Meanwhile, A PCV2d isolate with the estimated titre of 10.sup.5 TCID50/ml was serially diluted to generate the virus dilutions with the theoretical titres of 10.sup.4, 10.sup.3, 10.sup.2, and 30 TCID50/ml. The viruses at these dilutions were further 10-fold serially diluted and inoculated into PK15 cells for titration (3 replicate wells per dilution). The results are shown below:

TABLE-US-00002 Theoretical titer of the PCV2d isolate at different dilutions ~10{circumflex over ( )}4 TCID50/mL ~10{circumflex over ( )}3 TCID50/mL ~10{circumflex over ( )}2 TCID50/mL ~30 TCID50/mL 10{circumflex over ( )} 0 + + + + + + + + + + + + 10{circumflex over ( )} 1 + + + + + + + + + + + + 10{circumflex over ( )} 2 + + + + + + + + + − − − 10{circumflex over ( )} 3 + + + + − − − − − − − − 10{circumflex over ( )} 4 − + − − − − − − − − − − 10{circumflex over ( )} 5 − − − − − − − − − − − − 10{circumflex over ( )} 6 − − − − − − − − − − − − 10{circumflex over ( )} 7 − − − − − − − − − − − − 5.  8 × 10{circumflex over ( )}4 TCID50/mL 5.  8 × 10{circumflex over ( )}3 TCID50/mL 3.16 × 10{circumflex over ( )}3 TCID50/mL 3.16 × 10{circumflex over ( )}2 TCID  0/mL Obtained titer of the PCV2d isolate at different dilutions indicates data missing or illegible when filed

[0041] This complementary information leads to validate the PCV2 titration and isolation assays.

Example 5. Detection of Porcine and Bovine Viruses Using Yero, BT and ST Cell Lines and Real-Time Qualitative PCR

[0042] Tests were performed according to 9CFR guideline and to technical document TD0981-145#01.

[0043] For qPCR, samples analysed were tested diluted 10-fold, 100-fold and 1000-fold. For the same reason described in certificate 145/20/TD0981/03 and related deviation form FI-2020-029, only results obtained with the dilution 100-fold due to matrix properties are used to validate the assay.

[0044] The in vitro cell culture assay was performed in 13 different batches no infectious particles of the following viruses were detected: Parainfuenzae 3 virus, Bovine Parainfluenzae 3 Virus, Bovine Viral Diarrhea Virus (BVDV), Bovine AdenoVirus 3 (BAV-3), Blue Tongue Virus (BTV), Bovine Parvovirus (BPV), Reovirus 3 (Reo3), Rabies Virus, Bovine Respiratory Syncytial Virus (BRSV), Transmissible GastroEnteritis Virus (TGEV), Porcine ParvoVirus (PPV), Porcine AdenoVirus (PAV), and Porcine Hemagglutinating Encephalomyelitis Virus (PHEV).

[0045] Porcine viruses were tested since the porcine starting material. Bovine viruses were testing for the lactose from bovine origin.