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Formulation and in vitro characterization of ciprofloxacin floating and bioadhesive extended-release tablets.

机译:环丙沙星漂浮和生物粘附缓释片剂的配制和体外表征。

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摘要

Ciprofloxacin is mainly absorbed in the proximal areas of the gastrointestinal tract. The purpose of our study was production of floating-bioadhesive tablets to lengthen the stay of drug in its absorption area. Effervescent tablets were made using sodium carboxymethyl cellulose (CMC), hydroxypropyl methylcellulose (HPMC), polyacrylic acid (AA), polymetacrylic acid (MAA), citric acid, and sodium bicarbonate. Tablets with 5% effervescent base had longer lag time than 10%. The type of polymer had no significant effect on the floating lag time. All tablets floated atop the medium for 23-24 hr. Increasing CMC caused higher mucoadhesion than AA (p < 0.05). All formulations showed a Higuchi, non-Fickian release mechanism. Tablets with 10% effervescent base, 80% CMC/20% HPMC, or 80% AA /20% MAA seemed desirable.
机译:环丙沙星主要吸收在胃肠道的近端区域。我们研究的目的是生产浮动生物粘附片剂,以延长药物在其吸收区域的停留时间。使用羧甲基纤维素钠(CMC),羟丙基甲基纤维素(HPMC),聚丙烯酸(AA),聚甲基丙烯酸(MAA),柠檬酸和碳酸氢钠制备泡腾片。含5%泡腾片的片剂的滞后时间比10%更长。聚合物的类型对漂浮滞后时间没有显着影响。所有片剂漂浮在培养基上23-24小时。 CMC的增加引起的粘膜粘附性高于AA(p <0.05)。所有制剂均显示出Higuchi非Fickian释放机制。含10%泡腾片,80%CMC / 20%HPMC或80%AA / 20%MAA的片剂似乎是可取的。

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