Madani Aqilah F, Syauqi Muhammad A, Permatasari Jihan A, Putri Annisa A, M Fadel, Permana Andi Dian
Faculty of Pharmacy, Hasanuddin University, Makassar 90245, South Sulawesi, Indonesia.
Faculty of Medicine, Hasanuddin University, Makassar 90245, South Sulawesi, Indonesia.
ACS Appl Bio Mater. 2024 Apr 15;7(4):2582-2593. doi: 10.1021/acsabm.4c00246. Epub 2024 Apr 3.
Telmisartan (TMN), an angiotensin receptor blocker (ARB) drug, is being considered as an alternative therapy for Alzheimer's disease (ALZ). However, when taken orally, its low water solubility leads to a low bioavailability and brain concentration. To overcome this problem, TMN was formulated as nanocrystals (NC), then incorporated into dissolving microneedles (DMN) to enhance drug delivery to the brain via the trigeminal route on the face. TMN-NC was formulated with 1% PVA using the top-down method and stirred for 12 h, producing the smallest particle size of 132 ± 11 nm and showing a better release profile, reaching 89.51 ± 7.52% (2 times greater than pure TMN). TMN-NC-DMN with a combination of 15% PVA and 25% PVP showed optimal mechanical strength and penetration ability; they could dissolve completely within 15 min, and their surface pH was safe for the skin. The permeation test of TMN-NC-DMN showed the highest concentration, reaching 285.80 ± 32.12 μg/mL, compared to TMN-DMN and patch control, which only reached 87.17 ± 11.24 and 94.00 ± 11.09 μg/mL, respectively. The TMN-NC-DMN combination showed better bioavailability and was found to be well-delivered to the brain without any irritation to the skin. Pharmacokinetic parameters had a significant difference ( > 0.05) compared to other preparations, making it a promising treatment for ALZ.
替米沙坦(TMN)是一种血管紧张素受体阻滞剂(ARB)药物,正被视为治疗阿尔茨海默病(ALZ)的替代疗法。然而,口服时,其低水溶性导致生物利用度低和脑内浓度低。为克服这一问题,将TMN制成纳米晶体(NC),然后将其掺入可溶解微针(DMN)中,以通过面部的三叉神经途径增强药物向脑内的递送。采用自上而下的方法,用1%聚乙烯醇(PVA)制备TMN-NC,并搅拌12小时,产生的最小粒径为132±11nm,释放曲线更好,达到89.51±7.52%(比纯TMN高2倍)。含有15%PVA和25%聚乙烯吡咯烷酮(PVP)组合的TMN-NC-DMN表现出最佳的机械强度和穿透能力;它们可在15分钟内完全溶解,其表面pH值对皮肤安全。TMN-NC-DMN的渗透试验显示浓度最高,达到285.80±32.12μg/mL,相比之下,TMN-DMN和贴剂对照分别仅达到87.17±11.24和94.00±11.09μg/mL。TMN-NC-DMN组合表现出更好的生物利用度,并且被发现能很好地递送至脑内,对皮肤无任何刺激。与其他制剂相比,药代动力学参数有显著差异(>0.05),使其成为治疗ALZ的有前景的疗法。