Weight Variability of Scored and Unscored Psychotropic Drug Tablets Split by a Uniquely Designed Tablet Splitting Device

2005 ◽  
Vol 40 (4) ◽  
pp. 321-325 ◽  
Author(s):  
Robert J. Nolly ◽  
Patrick Rodrigues ◽  
Laura Thoma

Tablets of three psychotropic drugs were split using a uniquely designed tablet splitting device, the Tru-Cut Multi-Tablet Cutter, and evaluated for weight variation utilizing criteria based on the United States Pharmacopeia (USP) <27> Uniformity of Dosage Units Content Uniformity Criteria. Whole tablets of Risperdal 2 mg and 4 mg, Paxil 20 mg and 40 mg, and Zoloft 100 mg were split by a device that positioned tablets in tablet specific disposable trays for splitting. Each half tablet weight was recorded utilizing a digital electronic balance. Weight variability was determined by comparing actual half tablet weight to theoretical half tablet weight and calculation of the relative standard deviation. Results showed half tablets of all drugs met the weight variation criteria resulting in uniform half tablet dosages as defined by the criteria.

1985 ◽  
Vol 53 (01) ◽  
pp. 116-117 ◽  
Author(s):  
R E Merton ◽  
A D Curtis ◽  
D P Thomas

SummaryHeparin samples from five manufacturers were assayed by the revised British Pharmacopoeia (BP) heparin assay and the results compared with those obtained using the activated partial thromboplastin time (APTT) assay. The United States Pharmacopeia (USP) reference heparin preparation and the 4th International Standard (IS) for heparin were also assayed by the two methods relative to the 3rd IS. The results obtained by the revised BP assay were in close agreement with those obtained by the APTT assay for all the heparins that were tested. The assays revealed that there is at least a 10% discrepancy between the International Unit for heparin and the USP unit.


1994 ◽  
Vol 77 (3) ◽  
pp. 756-757 ◽  
Author(s):  
Simon Chernomorsky

Abstract The reliability of the currently used quantitative assay for commercially available chlorophyllin copper complex is discussed. It was shown that optical measurements at 405 nm can overestimate the purity of the preparation by 16.4–49.5%. This conclusion is from comparative studies using spectrophotometry at 405 nm and elemental analysis (copper content) of chlorophyllin copper complex. Spectrophotometry at 630 nm resulted in closer agreement with data calculated from elemental analysis. These observations have to be taken into consideration by those involved in the manufacture and distribution of chlorophyllin copper complex as well as in the development of the United States Pharmacopeia compendial monograph for this preparation.


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