Enhancing physicochemical properties of hydrochlorothiazide with zwitterionic L-proline and 5-fluorocytosine cocrystals through mechanochemical synthesis

IF 3.8 3区 医学 Q2 CHEMISTRY, MEDICINAL Journal of pharmaceutical sciences Pub Date : 2025-02-01 DOI:10.1016/j.xphs.2024.12.004
Pollyana Pereira Firmino , Cecilia Carolina Pinheiro da Silva , Paulo Nunes , José Eduardo Gonçalves , Fabrizia Grepioni , Javier Ellena
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Abstract

Hydrochlorothiazide (HTZ) is a thiazide-type diuretic drug approved by the FDA in 1959 for treatment of hypertension and peripheral edema and has been used since. HTZ exhibits low solubility and low permeability, leading to variable oral bioavailability and limited intestinal drug permeability. For this reason, several attempts to improve HTZ physicochemical properties have been made during the past decades. In the broad frame of molecular crystal engineering, significant efforts and promising results in the quest for more effective solid/dosage forms of HTZ, including studies on polymorphism and cocrystals, are being developed. As part of these efforts, we report here two new cocrystals of HTZ with the zwitterionic l-proline and the prodrug 5-Fluorocytosine. Both cocrystals show improvement in solubility and permeability, suggesting that these new solid forms could be used as new drug candidates to deliver HTZ in the antihypertensive therapy.

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双阴离子l -脯氨酸和5-氟胞嘧啶共晶机械合成提高氢氯噻嗪的理化性能。
氢氯噻嗪(HTZ)是一种噻嗪类利尿剂,于1959年被FDA批准用于治疗高血压和外周水肿,并一直使用至今。HTZ具有低溶解度和低渗透性,导致口服生物利用度变化和肠道药物渗透性有限。由于这个原因,在过去的几十年里,已经进行了几次尝试来改善HTZ的物理化学性质。在分子晶体工程的大框架下,在寻找更有效的HTZ固体/剂型方面,包括多态性和共晶的研究,正在进行重大的努力和有希望的结果。作为这些努力的一部分,我们在这里报道了两种新的HTZ共晶与两性离子l -脯氨酸和前药5-氟胞嘧啶。这两种共晶的溶解度和通透性均有改善,表明这些新的固体形式可以作为抗高血压药物的候选药物。
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来源期刊
CiteScore
7.30
自引率
13.20%
发文量
367
审稿时长
33 days
期刊介绍: The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.
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