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Collaborative study to evaluate a reporter gene assay for recombinant human follicle-stimulating hormone bioactivity
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Lü-yin WANG, Ping LÜ, Hui ZHANG, Jing LI*, Cheng-gang LIANG*
Acta Pharmaceutica Sinica | 2023, 58(3) : 760 - 766
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Acta Pharmaceutica Sinica | 2023, 58(3): 760-766
Original Articles
Collaborative study to evaluate a reporter gene assay for recombinant human follicle-stimulating hormone bioactivity
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Lü-yin WANG, Ping LÜ, Hui ZHANG, Jing LI*, Cheng-gang LIANG*
Affiliations
  • Division of Hormone, National Institutes for Food and Drug Control, NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, Beijing 102629, China
Published: 2023-03-12 doi: 10.16438/j.0513-4870.2022-1074
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The goal of this work was to explore the prospect of standardized application of an in-vitro bioactivity assay for recombinant human follicle-stimulating hormone based on a reporter gene. The relative accuracy, intermediate precision, linearity and applicable range of the method were validated according to the General Rules of Chinese Pharmacopoeia 2020 edition Volume IV (9401). Three laboratories used this method to determine the in-vitro biological activities of six batches of drug product and three batches of drug substance manufactured by two different companies. The consistency of the potency determined by three laboratories, the intra-laboratory precision and inter-laboratory precision were analyzed. The method was optimized during the collaborative validation. The results of method validation meet the requirements of the General Rules of Chinese Pharmacopoeia 2020 edition Volume IV (9401). Aiming to resolve the problems found in the collaborative validation, the medium for cell seeding, the pre-diluted buffer solution of standard and sample, and the means of removing and discarding supernatant after stimulation were optimized. After optimization, there was no significant difference in the bioactivity among the different laboratories (P > 0.05), indicating statistical equivalency. Intra-laboratory and inter-laboratory precision were good and the geometric coefficient of variation (GCV%) were both less than 15%. In conclusion, the reporter gene assay has good intra-laboratory repeatability and inter-laboratory reproducibility and is suitable for analyzing recombinant human follicle-stimulating hormone drug product and drug substance by different manufacturers. It is expected to be used as a standardized method for the determination of the in-vitro bioactivity of such products.

biological activity  /  recombinant human follicle-stimulating hormone  /  reporter gene assay  /  method validation  /  collaborative validation
Lü-yin WANG, Ping LÜ, Hui ZHANG, Jing LI, Cheng-gang LIANG. Collaborative study to evaluate a reporter gene assay for recombinant human follicle-stimulating hormone bioactivity[J]. Acta Pharmaceutica Sinica, 2023 , 58 (3) : 760 -766 . DOI: 10.16438/j.0513-4870.2022-1074
Year 2023 volume 58 Issue 3
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doi: 10.16438/j.0513-4870.2022-1074
  • Receive Date:2022-09-23
  • Online Date:2025-11-21
  • Published:2023-03-12
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  • Received:2022-09-23
  • Revised:2022-12-25
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    Division of Hormone, National Institutes for Food and Drug Control, NHC Key Laboratory of Research on Quality and Standardization of Biotech Products, Beijing 102629, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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