Novel First-Generation Dissolution Models to Investigate the Release and Uptake of Oral Lymphotropic Drug Products

被引:0
|
作者
Yousef, Malaz [1 ]
Park, Chulhun [2 ]
Chacra, Nadia Bou [3 ]
Davies, Neal M. [1 ]
Loebenberg, Raimar [1 ]
机构
[1] Univ Alberta, Fac Pharm & Pharmaceut Sci, Katz Grp Rexall Ctr Pharm & Hlth Res, 11315-87 Ave, Edmonton, AB T6G 2T9, Canada
[2] Jeju Natl Univ, Coll Pharm, Jeju 63243, South Korea
[3] Univ Sao Paulo, Fac Pharmaceut Sci, Sao Paulo, Brazil
来源
AAPS PHARMSCITECH | 2024年 / 25卷 / 06期
关键词
Lymphatic uptake; Artificial chylomicrons; Dissolution model; Bioequivalence; Lipid dissolution; LYMPHATIC-SYSTEM; SOLUBILITY; DELIVERY; GELS;
D O I
10.1208/s12249-024-02866-y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Conventional dissolution tests only assess the aqueous release of drugs to ensure quality and performance, without indicating whether absorption occurs through the portal or the lymphatic circulation. To address this issue, this study aimed to develop novel first-generation dissolution models that could investigate the release and uptake of oral lymphotropic drugs and examine relevant formulation issues. Dissolution of three commercial lymphotropic drug products (Terbinafina, Apo-terbinafine, and Lamisil) was done using modified versions of USP Apparatus II and IV. The developed models contained a lymphatic compartment filled with artificial chylomicrons to account for absorption through intestinal lymphatic pathway. The various products exhibited different release profiles into the aqueous media and the lymphatic media across the two tested models. The modified USP IV apparatus demonstrated greater distinction in aqueous release patterns. However, the release pattern into the lymphatic media remained similar in both models. This work represents a progress in meeting the challenges posed by the increasing complexity of pharmaceutical products containing lipophilic drugs or formulations, and has the potential to contribute towards the development of in-vitro bioequivalence standards for formulations targeting intestinal lymphatics.
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页数:9
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