枸橼酸西地那非儿科口服制剂的临时制备

IF 1.1 Q4 PHARMACOLOGY & PHARMACY Pharmacia Pub Date : 2023-10-11 DOI:10.3897/pharmacia.70.e111611
Milen Dimitrov, Dilyana Georgieva, Valentina Petkova
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引用次数: 0

摘要

儿科人口由几个非常不同的亚组组成,每个亚组都有自己的特点。因此,儿童不能被认为是“小大人”。开发适合儿童的配方是一个复杂的过程,因为它必须考虑儿童时期发生的生理变化及其对药物吸收的影响。枸橼酸西地那非是一种治疗指标较窄的药物,用于儿科治疗肺动脉高压。在目前的工作中,技术方法的临时制备儿科口服形式含有柠檬酸西地那非的个性化治疗的儿童进行了研究。对制备的制剂进行了物理稳定性、微生物稳定性、使用稳定性和活性物质含量测定。在选定的储存条件下(室温25°C±5°C和在5°C±2°C的冰箱中),在整个稳定性监测期间,所有测试的口服制剂在外观方面保持不变。建立的pH值表明,在稳定性研究期间,配方保持化学稳定。所有配制的口服制剂中柠檬酸西地那非的含量均保持在95% w/v以上。证实了所制备的组合物的微生物质量。在对实验数据进行分析的基础上,提出了制备临时配方的合理策略。
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Extemporaneous preparation of paediatric oral formulations with sildenafil citrate
The paediatric population is composed of several very different subgroups, each with its own specific characteristics. For this reason, children cannot be considered “small adults”. The development of formulations suitable for children is a complex process, as it must consider the physiological changes that occur during childhood and the impact they have on the absorption of drugs. Sildenafil citrate is a drug with a narrow therapeutic index used in paediatrics to treat pulmonary hypertension. In the present work, technological approaches for extemporaneous preparation of paediatric oral forms containing sildenafil citrate for personalized therapy in children were studied. The prepared formulations were tested for physical and microbiological stability, in-use stability, and determination of active substance content. All tested oral formulations remained unchanged in terms of appearance during the entire period of stability monitoring at the selected storage conditions – room temperature 25 °C ± 5 °C and in a refrigerator at 5 °C ± 2 °C. The established pH values suggest that the formulations remained chemically stable during the stability study. The content of sildenafil citrate in all prepared oral formulations remained above 95% w/v. The microbiological quality of the prepared compositions was confirmed. Rational strategies for preparation of extemporaneous formulations were proposed based on the analysis of experimental data.
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来源期刊
Pharmacia
Pharmacia PHARMACOLOGY & PHARMACY-
CiteScore
2.30
自引率
27.30%
发文量
114
审稿时长
12 weeks
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