酮咯酸三甲胺漂浮压缩包衣迷你片的处方及药动学研究

Vemula Sk, Venisetty Rk, Veerareddy Pr
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引用次数: 4

摘要

本研究拟采用压缩包衣法制备酮咯酸Tromethamine (KTM)泡腾型漂浮微型片。迷你片剂具有片剂和多颗粒制剂(如颗粒)的优点。利用漂浮迷你片的主要原理,可以避免直接接触胃粘膜,并获得较长时间的低剂量,以减少KTM对胃的刺激作用。采用4 mm圆扁冲孔,羟丙基甲基纤维素和泡腾液包被,制备KTM微型片剂。对制备的片剂进行重量变化、厚度、脆性、硬度、药物含量、体外浮力、体外释放度等评价,并对最佳处方进行体内检验。制备的迷你片具有良好的理化特性。F3的控释时间为12 h(99.46±0.93%)和9.4 h (T80%=9.4 h),浮滞时间为12 h。F3在雄性白化病兔体内的药动学研究表明,与速释型核心微型片剂相比,F3的生物利用度和Cmax分别提高了2.25倍和1.35倍。因此,开发KTM泡腾压缩包被微型漂浮片是口服给药的最佳途径,以最大限度地提高治疗效果。
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Formulation and Pharmacokinetics of Ketorolac Tromethamine Floating Compression Coated Mini-Tablets
Present research is intended to develop the Ketorolac Tromethamine (KTM) effervescent floating mini-tablets using compression coating method. Mini-tablets have the advantages of both tablets and multiparticulate formulations such as pellets. The main principle of floating mini-tablets can be applied to decrease the irritant effect of KTM on the stomach by avoiding the direct contact with the gastric mucosa and obtaining a low dosage for prolonged periods. KTM mini-tablets were prepared using 4 mm round flat punches and compression coated with hydroxypropyl methylcellulose and effervescent mixture. The prepared tablets were evaluated for weight variation, thickness, friability, hardness, drug content, in vitro buoyancy and in vitro release and the best formulation was subjected to further in vivo examination. The prepared mini-tablets exhibited satisfactory physicochemical characteristics. Formulation F3 offered the best controlled drug release (99.46 ± 0.93% in 12 h and T80%=9.4 h) along with floating lag time 12 h. Pharmacokinetic studies of F3 formulation in male albino rabbits showed 2.25-fold higher bioavailability and 1.35-fold higher Cmax compared to immediate release core mini-tablets. Hence development of KTM effervescent compression-coated floating mini-tablets is the best way to give through oral route to maximize the therapy.
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