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加速预测稳定性研究在评估洗必泰临时制剂货架寿命中的应用。

Application of Accelerated Predictive Stability Studies in Extemporaneously Compounded Formulations of Chlorhexidine to Assess the Shelf Life.

机构信息

Departamento de Farmacia Galénica y Tecnología Alimentaria, Facultad de Farmacia, Univsersidad Complutense de Madrid, Plaza Ramón y Cajal, s/n, 28040 Madrid, Spain.

Instituto Universitario de Farmacia Industrial (IUFI), Facultad de Farmacia, Universidad Complutense de Madrid, Plaza Ramón y Cajal, s/n, 28040 Madrid, Spain.

出版信息

Molecules. 2023 Dec 4;28(23):7925. doi: 10.3390/molecules28237925.

Abstract

Industrially fabricated medicines have a well-defined shelf life supported by rigorous studies before their approval for commercialization. However, the shelf life of extemporaneous compounding topical formulations prepared at hospitals tends to be shorter, especially when no data are available to prove a longer stability period. Also, the storage conditions are unknown in many circumstances. Accelerated Predictive Stability (APS) studies have been shown to be a useful tool to predict in a faster and more accurate manner the chemical stability of extemporaneously compounded formulations requiring a minimum amount of formulation, thereby reducing the chemical drug waste per study. Shelf life will be allocated based on scientific data without compromising drug efficacy or safety. In this work, the APS approach was applied to the commercially available Cristalmina (CR) and an extemporaneously compounded formulation of chlorhexidine (DCHX). A different degradation kinetic was found between DCHX and CR (Avrami vs. zero-order kinetics, respectively). This can explain the different shelf life described by the International Council for Harmonisation of Technical Requirements Registration Pharmaceuticals Human Use (ICH) conditions between both formulations. A predicted stability for the DCHX solution was obtained from the extrapolation of the degradation rate in long-term conditions from the Arrhenius equation. The estimated degradation from the Arrhenius equation for DCHX at 5 °C, 25 °C, and 30 °C at 365 days was 3.1%, 17.4%, and 25.9%, respectively. The predicted shelf life, in which the DCHX content was above 90%, was 26.67 months under refrigerated conditions and 5.75 and 2.24 months at 25 and 30 °C, respectively. Currently, the Spanish National Formulary recommends a shelf life of no longer than 3 months at room temperature for DCHX solution. Based on the predicted APS and confirmed by experimental long-term studies, we have demonstrated that the shelf life of DCHX extemporaneously compounded formulations could be prolonged by up to 6 months.

摘要

工业化生产的药品在获得商业化批准前经过了严格的研究,具有明确的保质期。然而,医院制备的临时配制的局部制剂的保质期往往更短,特别是在没有数据证明更长的稳定期时。此外,在许多情况下,储存条件是未知的。加速预测稳定性(APS)研究已被证明是一种有用的工具,可以更快、更准确地预测临时配制的制剂的化学稳定性,所需的制剂量最少,从而减少每一项研究的化学药物浪费。保质期将根据科学数据确定,在不影响药物疗效或安全性的情况下。在这项工作中,APS 方法应用于市售的 Cristalmina(CR)和一种临时配制的洗必泰(DCHX)制剂。发现 DCHX 和 CR 之间存在不同的降解动力学(分别为 Avrami 型和零级动力学)。这可以解释两种制剂在国际人用药品注册技术要求协调会(ICH)条件下描述的不同保质期。通过从 Arrhenius 方程中推断出长期条件下的降解速率,可以得到 DCHX 溶液的预测稳定性。根据 Arrhenius 方程,DCHX 在 5°C、25°C 和 30°C 下,在 365 天时的估计降解率分别为 3.1%、17.4%和 25.9%。在冷藏条件下,DCHX 含量高于 90%的预测保质期为 26.67 个月,在 25°C 和 30°C 下分别为 5.75 个月和 2.24 个月。目前,西班牙国家处方集建议 DCHX 溶液在室温下的保质期不超过 3 个月。基于预测的 APS 并通过长期实验研究证实,我们已经证明,DCHX 临时配制制剂的保质期可以延长 6 个月。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c85/10708018/09b36278ab1d/molecules-28-07925-g001.jpg

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