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Autor:
Michele Georges Issa, Natalia Vieira de Souza, Bruna Wenyi Chuang Jou, Marcelo Dutra Duque, Humberto Gomes Ferraz
Publikováno v:
Pharmaceutics, Vol 14, Iss 5, p 892 (2022)
The development of extended-release dosage forms with adequate drug release is a challenge for pharmaceutical companies, mainly when the drug presents high solubility, as in Biopharmaceutics Classification System (BCS) class I. This study aimed to de
Externí odkaz:
https://doaj.org/article/45f897d9aac24cf0910014c15f3e6849