Material, compressional and tableting properties of ipomea batatas (sweet potato) starch co-processed with silicon dioxide

Q3 Pharmacology, Toxicology and Pharmaceutics ACTA Pharmaceutica Sciencia Pub Date : 2019-01-01 DOI:10.23893/1307-2080.aps.05722
L. Bakre, Damola Osibajo, G. Koiki, Oluyemisi Adebowale Bamiro
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引用次数: 6

Abstract

This study aims to co-process native Ipomea batatas starch (NPS) with colloidal silicon dioxide and evaluate the properties of the co-processed excipient (CPS). The powder morphology was determined by scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and X-Ray Diffraction (XRD) measurements. The compressional, mechanical and release properties of metronidazole tablet formulations were evaluated. NPS was predominantly oval in shape while CPS had more large truncated ellipsoidal granules. Both NPS and CPS exhibited spectra typical of a Type A XRD pattern, but CPS has a sharp peak with strong intensity at 270 2q which was absent in NPS. Although NPS had a faster onset of plastic deformation, the overall amount of plastic deformation was higher in CPS. Tablets formulated with CPS had faster dissolution than those containing similar concentration of NPS. The co-processing of Ipomea batatas starch with colloidal silicon dioxide resulted in modification of its powder and tableting properties.
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与二氧化硅共加工的甘薯淀粉的材料、压缩和压片性能
本研究旨在利用胶体二氧化硅对天然伊波麦巴塔塔淀粉(NPS)进行共加工,并对共加工赋形剂(CPS)的性能进行评价。采用扫描电子显微镜(SEM)、差示扫描量热仪(DSC)和x射线衍射仪(XRD)测定粉末形貌。对甲硝唑片的压缩性能、力学性能和释放性能进行了评价。NPS主要呈椭圆形,而CPS则有较大的截形椭球状颗粒。NPS和CPS均表现出典型的a型XRD谱图,但CPS在270 2q处有一个尖峰,强度很强,这是NPS所没有的。虽然NPS的塑性变形开始更快,但CPS的总体塑性变形量更高。以CPS配制的片剂比同等浓度NPS配制的片剂溶出更快。将巴塔塔淀粉与胶体二氧化硅共加工,使其粉体性能和压片性能发生了改变。
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来源期刊
ACTA Pharmaceutica Sciencia
ACTA Pharmaceutica Sciencia Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.90
自引率
0.00%
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0
期刊介绍: Acta Pharmaceutica Sciencia (Acta Pharm. Sci.), formerly known as Bulletin of Pharmacy and Acta Pharmaceutica Turcica is a peer-reviewed scientific journal publishing current research and reviews covering all fields of pharmaceutical sciences since 1953. The original studies accepted for publication must be unpublished work and should contain data that have not been published elsewhere as a whole or a part. The reviews must provide critical evaluation of the state of knowledge related with the subject. All manuscripts has to be written in clear and concise English. Starting from 2016, the journal will be issued quarterly both in paper and on-line formates also publish special issues for national or international scientific meetings and activities in the coverage field.
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