| Submission to first decision
(The average time from manuscript submission to desk rejection, direct rejection/acceptance or assignment to the first editor) Note: For manuscripts that fully comply with the journal template. However, this timeframe does not apply to manuscripts with formatting or guideline deficiencies. If a manuscript is returned to the authors for corrections, the administrative review process will restart from the re-submission date. |
3 weeks |
|---|---|
| Submission to decision after review (For papers that are sent to review, the average time from submission to receipt of first editor decision) | 6 weeks |
| Submission to final decision (The average time from manuscript submission to the final editorial decision) | 16 weeks |
| Submission to publication (The average time from acceptance to publication. Manuscript published in early view are also included in this calculation) | 24 weeks |
ACTA Pharmaceutica Sciencia
2021 , Vol 59 , Num 4
Comparative in vitro Dissolution Study of Clonazepam Tablets of Bangladesh by UV-Visible Spectrophotometry
1 Department of Pharmacy, Brac University, Bangladesh2 Department of Pharmaceutical Technology, Institute for Pharmaceutical Skill Development and Research, Bangladesh
3 Department of Pharmacy, University of Asia Pacific, Bangladesh
4 Department of Pharmacy, State University of Bangladesh
DOI : 10.23893/1307-2080.APS.05940 Viewed : 18933 - Downloaded : 6701 This study was aimed to assess the pharmaceutical equivalence of four brands of clonazepam tablets available in Bangladesh using in vitro dissolution study by UV spectrophotometry. Dissolution study in water was carried out using USP type-2 paddle apparatus. Other quality control tests like weight variation, disintegration time and assay were also performed according to the established methods. Almost all the samples attained 85% drug dissolution within 15 minutes. The assay revealed that all brands contained around 94-107% (w/w) of labeled chemical content. All brands complied with the official specifications for disintegration time. Dissolution results of all the test products were compared to that of the reference product with difference factor (f1) and similarity factor (f2). Apart from brand B, the dissolution profiles of other brands showed no significant variations. The study indicates that brands C, D and E were equivalent to the reference brand A so they may be prescribed interchangeably. Keywords : Clonazepam, dissolution, disintegration, pharmaceutical equivalence