Ahmed Tarek A, Alay Asmaa M S, Okbazghi Solomon Z, Alhakamy Nabil A
Faculty of Pharmacy, Department of Pharmaceutics, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
Faculty of Pharmacy, Department of Pharmaceutics and Industrial Pharmacy, Al-Azhar University, Cairo, Egypt.
Dose Response. 2020 May 7;18(2):1559325820923859. doi: 10.1177/1559325820923859. eCollection 2020 Apr-Jun.
Dapoxetine (DPX) is an orally administered drug for the treatment of premature ejaculation (PE). One of the challenges of administering DPX orally as a tablet is its poor bioavailability (ie, 42%) due to extensive first-pass metabolism. Thus, it is vital to develop a new formulation and mode of delivery to achieve the unmet needs of PE treatment. In this study, an optimized DPX polymeric nanoparticle (PNP) was developed and subsequently loaded into a transdermal film. The Box-Behnken design was utilized to optimize 3 formulation factors affecting the particle size and entrapment efficiency (EE) of chitosan (CS)-alginate (ALG) PNPs. A 3-level factorial design was used to study the effect of 2 variables affecting DPX cumulative percent released and percent elongation from transdermal films loaded with DPX-PNPs. Permeation parameters were calculated following ex vivo permeation study through rat skin. Transport of the PNPs across the skin layers was investigated using a fluorescence laser microscope. Results revealed that an optimized PNPs formulation was developed with a particle size 415.94 nm and EE 37.31%. Dapoxetine was successfully entrapped in the polymeric matrix. Chitosan and ALG interacted electrostatically with the studied cross-linking agents to form a polyelectrolyte complex. The ex vivo study illustrated a sustained release profile of DPX with enhanced skin permeation from the film loaded PNPs. Moreover, the PNPs was able to penetrate deeper into skin layers. Therefore, DPX transdermal film developed in this work could be considered as a successful drug delivery with better patient compliance for the treatment of PE.
达泊西汀(DPX)是一种口服用于治疗早泄(PE)的药物。口服达泊西汀片剂面临的挑战之一是由于广泛的首过代谢,其生物利用度较差(即42%)。因此,开发一种新的制剂和给药方式以满足早泄治疗未满足的需求至关重要。在本研究中,开发了一种优化的达泊西汀聚合物纳米颗粒(PNP),随后将其负载到透皮薄膜中。采用Box-Behnken设计优化影响壳聚糖(CS)-海藻酸盐(ALG)PNP粒径和包封率(EE)的3个制剂因素。采用三水平析因设计研究影响负载DPX-PNP的透皮薄膜中DPX累积释放百分比和伸长百分比的2个变量的效应。通过大鼠皮肤的离体渗透研究后计算渗透参数。使用荧光激光显微镜研究PNP跨皮肤层的转运。结果显示,开发出了一种优化的PNP制剂,其粒径为415.94 nm,包封率为37.31%。达泊西汀成功包封在聚合物基质中。壳聚糖和海藻酸盐与所研究的交联剂发生静电相互作用形成聚电解质复合物。离体研究表明,DPX具有持续释放特性,且负载PNP的薄膜的皮肤渗透性增强。此外,PNP能够更深地渗透到皮肤层中。因此,本研究中开发的DPX透皮薄膜可被视为一种成功的药物递送方式,对早泄治疗具有更好的患者依从性。