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In Vivo Drug Dissolution in Human Oral Cavity from Orally Disintegrating Tablet and Comparability with in Vitro Testing

机译：在人口腔中的药物溶解，从口服崩解片剂和与的可比性进行测试

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Tsuyoshi Katayama; Shinya Uchida; Chiaki Kamiya; Shimako Tanaka; Yasuharu Kashiwagura; Akio Hakamata; Keiichi Odagiri; Naoki Inui; Hiroshi Watanabe; Noriyuki Namiki;
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1. In Vivo Drug Dissolution in Human Oral Cavity from Orally Disintegrating Tablet and Comparability with in Vitro Testing [J] . Tsuyoshi Katayama, Shinya Uchida, Chiaki Kamiya, Chemical and Pharmaceutical Bulletin . 2018,第10期

机译：口腔崩解片在人口腔中的体内药物溶解及其与体外测试的可比性
2. In Vivo Drug Dissolution in Human Oral Cavity from Orally Disintegrating Tablet and Comparability with in Vitro Testing [J] . Tsuyoshi Katayama, Shinya Uchida, Chiaki Kamiya, Chemical and Pharmaceutical Bulletin . 2018,第10期

机译：口腔崩解片在人口腔中的体内药物溶解及其与体外测试的可比性
3. In Vivo Drug Dissolution in Human Oral Cavity from Orally Disintegrating Tablet and Comparability with in Vitro Testing [J] . Katayama Tsuyoshi, Uchida Shinya, Kamiya Chiaki, Chemical and Pharmaceutical Bulletin . 2018,第10期

机译：在人口腔中的体内药物溶解，从口服崩解片剂和体外测试的可比性
4. In – vitro and in – vivo Evaluation of Nimesulide Lyophilized Orally Disintegrating Tablets [C] . Annual meeting exposition of the Controlled Release Society . 2009

机译：尼美冻干口腔崩解片剂的体外和体内评价
5. In-vitro, in-vivo and in-silico models in oral drug delivery and their relevance to human gastrointestinal physiology. [D] . Merchant, Hamid Ali. 2012

机译：口服药物递送的体外，体内和计算机模拟模型及其与人体胃肠道生理的关系。
6. Development of orally disintegrating tablets containing solid dispersion of a poorly soluble drug for enhanced dissolution: [O] . Shahinaze A. Fouad, Fady A. Malaak, Mohamed A. El-Nabarawi, 2020

机译：含有含有较差的溶解溶解的溶于溶解性较差的药物的口腔崩解片剂的研制性崩解片：
7. Evaluation of Oral Disintegration Time of Rapidly Disintegrating Tablets (RDTs) by In Vivo and In Vitro Disintegration Testing [O] . Keishi Yamasaki, Masashi Nagata, Rie Sato, 2006

机译：在体内和体外崩解测试中评价快速崩解片（RDT）的口服崩解时间
8. Guidance for Industry: SUPAC-MR: Modified Release Solid Oral Dosage Forms. Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation [R] . 1997

机译：行业指南：sUpaC-mR：改良释放固体口服剂型。放大和批准后的变化：化学，制造和控制;体外溶出度测试和体内生物等效性文档

In Vivo Drug Dissolution in Human Oral Cavity from Orally Disintegrating Tablet and Comparability with in Vitro Testing

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