Mirzaeei Shahla, Faryadras Fatemeh Bahrami, Mehrandish Saba, Rezaei Leila, Daneshgar Farid, Karami Ahmad
Pharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, I.R. Iran.
Nano Drug Delivery Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, I.R. Iran.
Res Pharm Sci. 2022 Sep 8;17(5):468-481. doi: 10.4103/1735-5362.355196. eCollection 2022 Oct.
Prolonging the drug release can be a suitable approach to overcome the challenges related to topical ophthalmic administration of drugs especially the ones prescribed for chronic ailments. The sustained delivery of the drug would reduce the required frequency of administration which could extremely improve patient compliance and feeling of well-being. This study aimed to develop nanofibrous inserts for sustained ophthalmic delivery of timolol maleate (TIM) for the treatment of glaucoma.
Polycaprolactone-based nanofibers containing TIM were prepared using pure polycaprolactone or a blend of it with cellulose acetate or Eudragit RL100 polymers by the electrospinning method. Following the preparation, polymeric inserts were evaluated for morphological and physicochemical properties. The drug release was assessed and the efficacy of a selected insert in decreasing the intraocular pressure (IOP) was also evaluated in the equine eyes.
FINDINGS / RESULTS: Prepared nanofibers indicated diameter ranged between 122-174 nm. The formulations showed suitable physicochemical properties and stability for ophthalmic administration. release study showed prolonged release of drug during more than 3 days. evaluation revealed that the prepared insert is non-irritant and non-toxic to the equine eyes while having suitable efficacy in decreasing the IOP during 6 days.
Prepared TIM inserts indicated a higher efficacy than commercial TIM eye drop in lowering IOP during a prolonged period. Thus, these formulations can be considered suitable for enhancing patient compliance by reducing the frequency of administration in the treatment of glaucoma.
延长药物释放可能是克服与局部眼部给药相关挑战的一种合适方法,尤其是针对慢性疾病所开的药物。药物的持续递送将减少所需的给药频率,这可极大地提高患者的依从性和幸福感。本研究旨在开发用于马来酸噻吗洛尔(TIM)眼部持续递送以治疗青光眼的纳米纤维插入物。
通过静电纺丝法,使用纯聚己内酯或其与醋酸纤维素或尤特奇RL100聚合物的混合物制备含TIM的聚己内酯基纳米纤维。制备后,对聚合物插入物的形态和物理化学性质进行评估。评估药物释放情况,并在马眼中评估所选插入物降低眼压(IOP)的功效。
制备的纳米纤维直径在122 - 174纳米之间。这些制剂显示出适合眼部给药的物理化学性质和稳定性。释放研究表明药物在3天以上的时间内持续释放。评估显示,制备的插入物对马眼无刺激性和毒性,同时在6天内具有降低眼压的合适功效。
制备的TIM插入物在长时间降低眼压方面显示出比市售TIM滴眼液更高的功效。因此,这些制剂可被认为适合通过减少青光眼治疗中的给药频率来提高患者依从性。