scholarly journals On combining estimates of relative potency in bioassay

1962 ◽  
Vol 60 (3) ◽  
pp. 379-385 ◽  
Author(s):  
B. M. Bennett
Keyword(s):  
Relative Potency ◽  
Confidence Limits ◽  
Biological Assays ◽  
Standard Preparation ◽  
Combining Estimates ◽  
Quantitative Response ◽  
Bio Assay ◽  
Tests Of Linear Hypotheses

Biological assays based on a quantitative response in particular (e.g. hormone assays) typically involve the estimation of (log) relative potency (= M) with respect to some standard preparation on the basis of one or more symmetrical determinations usually at equally spaced (log) dose intervals. It is the purpose of this paper to consider further statistical aspects of estimates of M, and especially confidence limits for M based on a combination of separate assays. These are given as examples of tests of linear hypotheses. Two applications are given on the combining of quantitative bio-assay data.

Analysis of Fat-Soluble Vitamins. XVI. Antirachitic Activity of 5,6-trans-Vitamin D3 Alone and in the Presence of 5,6-cis-Vitamin D3 Resin, Using Chick Bioassays

1977 ◽  
Vol 60 (5) ◽  
pp. 1003-1009
Author(s):  
Ben Borsje ◽  
Arend Heyting ◽  
Jan R Roborgh ◽  
David B Ross ◽  
Kenneth W G Shillam
Keyword(s):  
Trans Isomer ◽  
Vitamin D3 ◽  
Relative Potency ◽  
Biological Assays ◽  
Fat Soluble Vitamins ◽  
Cis Isomer

Abstract Two biological assays were conducted in which the antirachitic activity in chicks of 5,6-trans-vitamin D3 added to feed is compared with that of 5,6-cis-vitamin D3. On the basis of the results obtained it is concluded that the relative potency of the trans isomer is, at the most, 5% and that the antirachitic activity of the trans isomer is not markedly enhanced (an increase to a relative potency of 16%, at the most) if the cis isomer is also included in the diet. The results are not conclusive on the inhibition or lack of inhibition of the antirachitic activity of 5,6-cis-vitamin D3 by the presence of 5,6-trans-vitamin D3 in the feed.

Confidence Limits for Biological Assays

1945 ◽  
Vol 1 (5) ◽  
pp. 57 ◽  
Author(s):  
C. I. Bliss
Keyword(s):  
Confidence Limits ◽  
Biological Assays

Structural similarity of ribosomes from E. coli and A. salina

1978 ◽  
Vol 36 (2) ◽  
pp. 242-243
Author(s):  
M. Boublik ◽  
R.M. Wydro ◽  
W. Hellmann ◽  
F. Jenkins
Keyword(s):  
Ribosomal Proteins ◽  
Direct Evidence ◽  
Structural Similarity ◽  
Carbon Support ◽  
Artemia Salina ◽  
Uranyl Acetate ◽  
Biological Assays ◽  
E Coli ◽  
And Function ◽  
Fine Carbon

Ribosomes are ribonucleoprotein particles necessary for processing the genetic information of mRNA into proteins. Analogy in composition and function of ribosomes from diverse species, established by biochemical and biological assays, implies their structural similarity. Direct evidence obtained by electron microscopy seems to be of increasing relevance in understanding the structure of ribosomes and the mechanism of their role in protein synthesis.The extent of the structural homology between prokaryotic and eukaryotic ribosomes has been studied on ribosomes of Escherichia coli (E.c.) and Artemia salina (A.s.). Despite the established differences in size and in the amount and proportion of ribosomal proteins and RNAs both types of ribosomes show an overall similarity. The monosomes (stained with 0.5% aqueous uranyl acetate and deposited on a fine carbon support) appear in the electron micrographs as round particles with a diameter of approximately 225Å for the 70S E.c. (Fig. 1) and 260Å for the 80S A.s. monosome (Fig. 2).

A in Vivo Assay for Standardizing Heparin Preparations

1979 ◽  
Vol 41 (03) ◽  
pp. 576-582
Author(s):  
A R Pomeroy
Keyword(s):  
In Vitro Assays ◽  
British Pharmacopoeia ◽  
In Vitro Method ◽  
Standard Preparation ◽  
Reliable Estimation ◽  
Assay Procedure ◽  
Accuracy And Precision ◽  
Heparin Preparation

SummaryThe limitations of currently used in vitro assays of heparin have demonstrated the need for an in vivo method suitable for routine use.The in vivo method which is described in this paper uses, for each heparin preparation, four groups of five mice which are injected intravenously with heparin according to a “2 and 2 dose assay” procedure. The method is relatively rapid, requiring 3 to 4 hours to test five heparin preparations against a standard preparation of heparin. Levels of accuracy and precision acceptable for the requirements of the British Pharmacopoeia are obtained by combining the results of 3 to 4 assays of a heparin preparation.The similarity of results obtained the in vivo method and the in vitro method of the British Pharmacopoeia for heparin preparations of lung and mucosal origin validates this in vivo method and, conversely, demonstrates that the in vitro method of the British Pharmacopoeia gives a reliable estimation of the in vivo activity of heparin.

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