Open Access Repository

Comparative FTIR, compaction and In vitro dissolution studies of Plectranthus esculentus modified starches in metronidazole tablet formulations by direct compression


Downloads per month over past year

Khalid, GM, Musa, H, Olowosulu, AK, Jatau, AI, Ilyasu, S and Gawarzo, MS 2018 , 'Comparative FTIR, compaction and In vitro dissolution studies of Plectranthus esculentus modified starches in metronidazole tablet formulations by direct compression' , Pharmaceutica Analytica Acta, vol. 9, no. 1 , pp. 1-9 , doi: 10.4172/2153-2435.1000578.

PDF (Published version)
ComparativeFTIR...pdf | Download (745kB)

| Preview


Wet and dry granulation methods for tablet manufacturing tend to be problematic for thermolabile and moisturesensitive drugs, and few excipients are available for use in direct compression (DC) due to stringent requirements.This study aimed to evaluate the drug/excipients compatibility, compaction and in vitro dissolution properties ofPlectranthus esculentus modified starches in tablets using metronidazole as a model drug by DC. Native starchextracted from P. esculentus was modified by three methods and we produced three modified starches namely;acid hydrolyzed P. esculentus starch (APS), pregelatinized P. esculentus starch (PPS), and ethanol dehydratedpregelatinized P. esculentus starch (PPE). For drug/excipient compatibility studies, Fourier Transform InfraredSpectroscopy (FTIR) was used. Powder compaction was evaluated using Heckel model, while in vitro dissolutionstudies were conducted using USP basket method. The starches were evaluated in comparison with microcrystallinecellulose (MCC PH 101). The FTIR peaks revealed no interaction of these excipients with the drug. Compactionstudies indicate that the modifications yielded starches of comparable compact behaviors with MCC PH 101especially APS and PPE, they both plastically deformed with PPE producing the hardest tablets. APS and PPSdisintegrate faster 2.83 and 1.42 min respectively which were significantly different from the disintegration time ofMCC PH 101 and PPE which are higher 35.34 and 45.53 min respectively. For the in vitro dissolution, APS and PPS,their T50 and T90 were achieved in less than 10 min, T50 and T90 for PPE were achieved at 38 and 58 min respectively,while for MCC PH 101 both T50 and T90 were not observed after 60 min. APS produced metronidazole tablets ofbetter quality in terms crushing strength, friability and drug-release profile. Acid hydrolysis of P. esculentus starchproduced good directly compressible excipient that can be use in DC for immediate release tablet formulations.

Item Type: Article
Authors/Creators:Khalid, GM and Musa, H and Olowosulu, AK and Jatau, AI and Ilyasu, S and Gawarzo, MS
Keywords: <i>Plectranthus esculentus</i>, modified starch, FTIR, dissolution, compaction, tablet
Journal or Publication Title: Pharmaceutica Analytica Acta
Publisher: Longdom Group SA
ISSN: 2153-2435
DOI / ID Number: 10.4172/2153-2435.1000578
Copyright Information:

Copyright: © 2018 Khalid GM, et al. This is an open-access article distributedunder the terms of the Creative Commons Attribution License, which permitsunrestricted use, distribution, and reproduction in any medium, provided theoriginal author and source are credited.

Item Statistics: View statistics for this item

Actions (login required)

Item Control Page Item Control Page