聚合物、表面活性剂和其他辅料对萘普生钠从制备的基质中释放的影响以及这些添加剂对片剂溶胀率的影响。

Q4 Medicine International journal of pharmaceutical compounding Pub Date : 2023-09-01
Hassan Alhmoud, Yazan Akkam, Derar Omari, Alaa Alghananim, Mohammad Bani Melhem
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引用次数: 0

摘要

本研究旨在利用亲水性聚合物羧甲基纤维素钠制备萘普生控释基质片,研究表面活性剂和其他辅料对药物释放和溶胀率的影响,并确定药物释放机制。采用直接压片技术,将不同比例的羧甲基纤维素钠和其他辅料配制成萘普生基质。使用酸性溶解介质评估药物释放、溶胀行为和释放机制。通过拟合零阶、一阶、Higuchi和Korsmeyer-Peppas模型来表征药物释放速率和机制。聚合物羧甲基纤维素钠和其他添加剂的量通过根据聚合物羧甲基纤维钠的比例调节其速率来显著影响药物释放。表面活性剂基于其溶解度和润湿作用而增加药物释放,与它们的电荷无关。释放机制包括聚合物扩散和片剂在溶解过程中的侵蚀。本研究表明,通过直接压片将聚合物羧甲基纤维素钠和其他赋形剂结合,可以有效地制备萘普生控释基质片。赋形剂的量可以调节以控制药物从基质的释放速率。溶解介质和表面活性剂不影响基质溶胀,而表面活性剂通过溶解度和润湿作用而不是电荷来增加药物释放。这些发现对控释药物递送系统的设计和开发具有重要意义。
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The Influence of Polymers, Surfactants, and Other Excipients on Naproxen Sodium Release from Matrices Prepared and the Effect of These Additives on the Swelling Rate of the Tablet.

This study aimed to develop controlled-release matrix tablets of naproxen using the hydrophilic polymer sodium carboxymethylcellulose, investigate the impact of surfactants and other excipients on drug release and swelling rate, and determine the drug release mechanism. Naproxen matrices were formulated by the direct compression technique with different ratios of polymer sodium carboxymethylcellulose and other excipients. Drug release, swelling behavior, and release mechanism were assessed using an acidic dissolution medium. Drug release rate and mechanism were characterized by fitting the zero-order, first-order, Higuchi, and Korsmeyer-Peppas models. The amount of polymer sodium carboxymethylcellulose and other additives significantly affected drug release by regulating its rate according to polymer sodium carboxymethylcellulose ratios. Surfactants increased the drug release based on their solubility and wetting effects, independent of their charges. The release mechanism involved a combination of polymer diffusion and tablet erosion during dissolution. This study demonstrated that controlled release matrix tablets of naproxen can be effectively prepared by incorporating polymer sodium carboxymethylcellulose and other excipients via direct compression. The quantity of excipients can be adjusted to control the drug release rate from the matrices. The dissolution medium and the surfactants did not affect the matrix swelling, while the surfactants increased drug release via solubility and wetting effects rather than their charge. These findings have important implications for the design and development of controlled-release drug delivery systems.

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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
62
期刊介绍: The International Journal of Pharmaceutical Compounding (IJPC) is a bi-monthly, scientific and professional journal emphasizing quality pharmaceutical compounding. IJPC is the only publication that covers pharmaceutical compounding topics relevant and necessary to empower pharmacists to meet the needs of today"s patients. No other publication features hands-on, how-to compounding techniques or the information that contemporary pharmacists need to provide individualized care.
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