Quantitation of human chorionic gonadotrophin (hCG) by radioreceptor assay
✍ Scribed by Lars Sjödin; Hans Dahlén; Kristina Erlandsson-Persson; Anne-Charlotte Henningsson; Eila Viitanen
- Book ID
- 103911317
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 627 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0731-7085
No coin nor oath required. For personal study only.
✦ Synopsis
A sensitive radioreceptor assay was developed for pharmaceutical preparations of human chorionic gonadotrophin with the use of rat testicular membranes as receptor preparation and human 125I-chorionic gonadotrophin as tracer. The addition of unlabelled human chorionic gonadotrophin or luteinizing hormone inhibited the binding of 125I-chorionic gonadotrophin to the receptors in a concentration dependent way. Concentrations of human chorionic gonadotrophin between 30-300 mIU ml(-1) were normally used for a three-dose assay fulfilling pharmacopoeial statistical requirements for assay validity. The relative standard deviation for five assays was 7%. Estimates of potency of commercial preparations of human chorionic gonadotrophin obtained with the radioreceptor assay correlated well with corresponding estimates from in vivo assays. The proposed radioreceptor assay, however, provides a considerable saving in the number of animals required, requires less technical support, and is more precise than the in vivo method.
📜 SIMILAR VOLUMES
## In Chinese hamster ovary cells overexpressing Edg-1, one of the sphingosine 1-phosphate (S1P) receptor subtypes, [ 3 H]S1P binding was displaced by unlabeled S1P with IC 50 , a half-maximal concentration to inhibit the binding, of about 20 nM. This radioreceptor binding was used for quantitativ