Singh Mahendra, Kumar Sanjay, Vinayagam Ramachandran, Samivel Ramachandran
Department of Biotechnology, College of Life and Applied Sciences, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Formulation Research and Development, Naari Pharma Private Limited, Sec-5, Rudrapur 263153, India.
Pharmaceuticals (Basel). 2025 Jun 11;18(6):871. doi: 10.3390/ph18060871.
Non-invasive central nervous system (CNS) therapies are limited by complex mechanisms and the blood-brain barrier, but nasal delivery offers a promising alternative. The study planned to develop a non-invasive in situ intranasal mucoadhesive thermosensitive gel to deliver CNS-active risperidone via nose-to-brain targeting. Risperidone, a second-generation antipsychotic, has shown efficacy in managing both psychotic and mood-related symptoms. The mucoadhesive gel formulations help to prolong the residence time at the nasal absorption site, thereby facilitating the uptake of the drug. The poloxamer 407 (18.0% /), HPMC K100M and K15M (0.3-0.5% /), and benzalkonium chloride (0.1% /) were used as thermosensitive polymers, a mucoadhesive agent, and a preservative, respectively, for the development of in situ thermosensitive gel. The developed formulations were evaluated for various parameters. The pH, gelation temperature, gelation time, and drug content were found to be 6.20 ± 0.026-6.37 ± 0.015, 34.25 ± 1.10-37.50 ± 1.05 °C, 1.65 ± 0.30-2.50 ± 0.55 min, and 95.58 ± 2.37-98.03 ± 1.68%, respectively. Furthermore, the optimized F3 formulation showed satisfactory gelling capacity (9.52 ± 0.513 h) and an acceptable mucoadhesive strength (1110.65 ± 6.87 dyne/cm). Diffusion of the drug through the egg membrane depended on the formulation's viscosity, and the F3 formulation explained the first-order release kinetics, indicating concentration-dependent drug diffusion with < 0.45 (0.398) value, indicating the Fickian-diffusion (diffusional case I). The pharmacokinetic study was performed with male Wistar albino rats, and the F3 in situ thermosensitive risperidone gel confirmed significantly ( < 0.05) ~5.4 times higher brain AUC when administered intranasally compared to the oral solution. Based on physicochemical, in vitro, and in vivo parameters, it can be concluded that in situ thermosensitive gel is suitable for administration of risperidone through the nasal route and can enhance patient compliance through ease of application and with less repeated administration.
非侵入性中枢神经系统(CNS)疗法受到复杂机制和血脑屏障的限制,但鼻腔给药提供了一种有前景的替代方案。该研究计划开发一种非侵入性原位鼻内粘膜粘附热敏凝胶,通过鼻脑靶向递送中枢神经系统活性药物利培酮。利培酮是一种第二代抗精神病药物,已显示出在管理精神病性和情绪相关症状方面的疗效。粘膜粘附凝胶制剂有助于延长在鼻腔吸收部位的停留时间,从而促进药物的吸收。泊洛沙姆407(18.0%/)、羟丙甲纤维素K100M和K15M(0.3 - 0.5%/)以及苯扎氯铵(0.1%/)分别用作热敏聚合物、粘膜粘附剂和防腐剂,用于开发原位热敏凝胶。对开发的制剂进行了各种参数的评估。发现pH值、胶凝温度、胶凝时间和药物含量分别为6.
20±0.026 - 6.37±0.015、34.25±1.10 - 37.50±1.05℃、1.65±0.30 - 2.50±0.55分钟和95.58±2.37 - 98.03±1.68%。此外,优化后的F3制剂显示出令人满意的胶凝能力(9.52±0.513小时)和可接受的粘膜粘附强度(1110.65±6.87达因/厘米)。药物通过卵膜的扩散取决于制剂的粘度,F3制剂符合一级释放动力学,表明药物扩散与浓度有关, 值<0.45(0.398),表明为菲克扩散(扩散情况I)。在雄性Wistar白化大鼠上进行了药代动力学研究,与口服溶液相比,鼻内给药时F3原位热敏利培酮凝胶的脑药时曲线下面积(AUC)显著高出约5.4倍(<0.05)。基于物理化学、体外和体内参数,可以得出结论,原位热敏凝胶适用于通过鼻腔途径给药利培酮,并且可以通过易于应用和减少重复给药来提高患者的依从性。