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Pregelatinized glutinous rice starch as a sustained release agent for tablet preparations

机译:预胶化糯米淀粉作为片剂制剂的缓释剂

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The aim of this study was to modify the glutinous rice starch (GS) as a sustained release agent for tablet preparations. The GS slurry was physically modified by heat and then dried by spray drying. The pregelatinized GS (PCS) appeared in odorless fine white powder. Its flowability is extremely poor. The tablet containing PCS and propranolol HCl were prepared by wet granulation method. Less than 80% of propranolol HCl was released in the period of 10 h at the drug to PGS ratio of 1:2 and longer than 14 h at the ratios of 1:3 and 1:4. The higher the composition ratio of PGS, the slower the release of the drug. The mechanisms of drug release from the matrices were anomalous (non-Fickian) diffusion in both hydrochloric buffer (pH 1.2) and phosphate buffer media (pH 6.8). The compaction pressure in the range of 6.9-27.5 MPa does not affect the release of the drug from the matrices.
机译:这项研究的目的是修饰糯米淀粉(GS)作为片剂制剂的缓释剂。 GS浆料通过加热进行物理改性,然后通过喷雾干燥进行干燥。预胶化的GS(PCS)以无味的白色细粉末出现。其流动性极差。通过湿法制粒制备含有PCS和盐酸普萘洛尔的片剂。在10小时内,药物与PGS的比例为1:2时,盐酸普萘洛尔释放的少于80%,而在1:3和1:4的比例下,则释放14小时以上。 PGS的组成比越高,药物的释放越慢。药物从基质中释放的机制是在盐酸缓冲液(pH 1.2)和磷酸盐缓冲液(pH 6.8)中的异常扩散(非Fickian扩散)。压实压力在6.9-27.5 MPa的范围内,不会影响药物从基质中的释放。

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