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用于儿科的卡维地洛口服溶液制剂的研发。

Development of a Carvedilol Oral Liquid Formulation for Paediatric Use.

作者信息

Chiclana-Rodríguez Blanca, Garcia-Montoya Encarnacion, Rouaz-El Hajoui Khadija, Romero-Obon Miquel, Nardi-Ricart Anna, Suñé-Pou Marc, Suñé-Negre Josep M, Pérez-Lozano Pilar

机构信息

Department of Pharmacy and Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII, 27-31, 08028 Barcelona, Spain.

Pharmacotherapy, Pharmacogenetics and Pharmaceutical Technology Research Group, Bellvitge Biomedical Research Institute (IDIBELL), Av. Gran Via de l'Hospitalet, 199-203, 08090 Barcelona, Spain.

出版信息

Pharmaceutics. 2023 Sep 5;15(9):2283. doi: 10.3390/pharmaceutics15092283.

Abstract

Carvedilol (CARV) is an 'off-label' β-blocker drug to treat cardiovascular diseases in children. Since CARV is nearly insoluble in water, only CARV solid forms are commercialized. Usually, CARV tablets are manipulated to prepare an extemporaneous liquid formulation for children in hospitals. We studied CARV to improve its aqueous solubility and develop an oral solution. In this study, we assessed the solubility and preliminary stability of CARV in different pH media. Using malic acid as a solubility enhancer had satisfactory results. We studied the chemical, physical, and microbiological stability of 1 mg/mL CARV-malic acid solution. A design of experiment (DoE) was used to optimize the CARV solution's preparation parameters. A 1 mg/mL CARV solution containing malic acid was stable for up to 12 months at 25 °C and 30 °C and 6 months at 40 °C. An equation associating malic acid with CARV concentrations was obtained using DoE. Microbiological data showed that the use of methylparaben was not necessary for this period of time. We successfully developed an aqueous CARV solution suitable for paediatrics and proven to be stable over a 12-month period.

摘要

卡维地洛(CARV)是一种用于治疗儿童心血管疾病的“非标签”β受体阻滞剂药物。由于卡维地洛几乎不溶于水,只有其固体剂型实现了商业化。通常,医院会对卡维地洛片剂进行处理,以制备用于儿童的临时液体制剂。我们对卡维地洛进行了研究,以提高其水溶性并开发一种口服溶液。在本研究中,我们评估了卡维地洛在不同pH介质中的溶解度和初步稳定性。使用苹果酸作为增溶剂取得了令人满意的结果。我们研究了1mg/mL卡维地洛-苹果酸溶液的化学、物理和微生物稳定性。采用实验设计(DoE)来优化卡维地洛溶液的制备参数。含苹果酸的1mg/mL卡维地洛溶液在25℃和30℃下可稳定保存长达12个月,在40℃下可稳定保存6个月。通过DoE获得了一个将苹果酸与卡维地洛浓度相关联的方程。微生物学数据表明,在此时间段内无需使用对羟基苯甲酸甲酯。我们成功开发了一种适用于儿科的卡维地洛水溶液,并证明其在12个月内稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/252b/10537783/39f03dd19932/pharmaceutics-15-02283-g001.jpg

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