Pivotal role of Acitretin nanovesicular gel for effective treatment of psoriasis: ex vivo-in vivo evaluation study

被引:73
作者
Abu Hashim, Irhan Ibrahim [1 ]
El-Magd, Noha Fawzy Abo [1 ]
El-Sheakh, Ahmed Ramadan [2 ]
Hamed, Mohammed Fawzy [3 ]
Abd El-Gawad, Abd El-Gawad Helmy [1 ]
机构
[1] Mansoura Univ, Dept Pharmaceut, Fac Pharm, El Gomhoria St, Mansoura 35516, Egypt
[2] Mansoura Univ, Dept Pharmacol & Toxicol, Fac Pharm, Mansoura, Egypt
[3] Mansoura Univ, Dept Pathol, Fac Vet Med, Mansoura, Egypt
关键词
Acitretin; nanovesicular gel; drug deposition; HaCaT cells; mouse tail model; antipsoriatic activity; NANOSTRUCTURED LIPID CARRIERS; DRUG-DELIVERY SYSTEMS; NONIONIC SURFACTANT VESICLES; HAIRLESS MOUSE SKIN; RETINOIC ACID; TRANSDERMAL DELIVERY; VITRO EVALUATION; STABILITY EVALUATION; TOPICAL TREATMENT; LOADED NIOSOMES;
D O I
10.2147/IJN.S156412
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
The goal of the current study was to explore the potential benefits of Acitretin (Act) nanovesicular gel as a prospective antipsoriatic topical delivery system counteracting the drug challenges in terms of its extremely low aqueous solubility, instability, skin irritation, and serious systemic adverse effects. Act-loaded niosomes were successfully developed, entirely characterized, and optimized. Further evaluation of the optimized formula was conducted regarding its stability and ex vivo cytotoxicity on different cell lines. The optimized niosomal vesicles were then incorporated in gel base matrix and investigated by sequential ex vivo (skin permeation and deposition) and in vivo (skin irritation and antipsoriatic activity using mouse tail model) experiments. The optimized Act-loaded niosomes (span 60: cholesterol molar ratio 1: 1) were spherical in shape and exhibited the highest entrapment efficiency (90.32 +/- 3.80%) with appropriate nanosize and zeta potential of 369.73 +/- 45.45 nm and -36.33 +/- 1.80 mV, respectively. Encapsulation of the drug in the nanovesicles was further emphasized by differential scanning calorimetric and powder X-ray diffraction studies. After 3 months storage at 4 +/- 1 degrees C, the optimized formula preserved its stability. Act nano niosomal gel produced a remarkable enhanced ex vivo permeation profile up to 30 h and significant drug deposition in the viable epidermal-dermal layers compared with those of Act gel. The pronounced antipsoriatic activity of the medicated nano niosomes was proved ex vivo in HaCaT cells (a keratinocyte cell line). Topical application of Act nano niosomal gel to mouse tail model further established its distinct in vivo antipsoriatic superiority in terms of significantly higher orthokeratosis, drug activity, and reduction in epidermal thickness compared with the control and other gel formulations. Also, negligible skin irritation and better skin tolerability of Act nanovesicular gel were revealed by primary irritation index and histopathologic examination.
引用
收藏
页码:1059 / 1079
页数:21
相关论文
共 111 条
[1]
Design and optimization of topical methotrexate loaded niosomes for enhanced management of psoriasis: Application of Box-Behnken design, in-vitro evaluation and in-vivo skin deposition study [J].
Abdelbary, Aly A. ;
AbouGhaly, Mohamed H. H. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2015, 485 (1-2) :235-243
[2]
Transfersomal Nanoparticles for Enhanced Transdermal Delivery of Clindamycin [J].
Abdellatif, Ahmed A. H. ;
Tawfeek, Hesham M. .
AAPS PHARMSCITECH, 2016, 17 (05) :1067-1074
[3]
Potential Use of Niosomal Hydrogel as an Ocular Delivery System for Atenolol [J].
Abu Hashim, Irhan Ibrahim ;
El-dahan, Marwa Salah ;
Yusif, Rehab Mohammed ;
Abd-ElGawad, Abd-ElGawad Helmy ;
Arima, Hidetoshi .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2014, 37 (04) :541-551
[4]
Preparation and in vitro evaluation of liposomal/niosomal delivery systems for antipsoriatic drug dithranol [J].
Agarwal, R ;
Katare, OP ;
Vyas, SP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 228 (1-2) :43-52
[5]
Development, evaluation and clinical studies of Acitretin loaded nanostructured lipid carriers for topical treatment of psoriasis [J].
Agrawal, Yogeeta ;
Petkar, Kailash C. ;
Sawant, Krutika K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 401 (1-2) :93-102
[6]
Ali MFM, 2015, DRUG DES DEV THER, V9, P2431, DOI [10.2147/DDDT.581236, 10.2147/DDDT.S81236]
[7]
Transdermal Delivery of Molecules is Limited by Full Epidermis, Not Just Stratum Corneum [J].
Andrews, Samantha N. ;
Jeong, Eunhye ;
Prausnitz, Mark R. .
PHARMACEUTICAL RESEARCH, 2013, 30 (04) :1099-1109
[8]
Increasing the intracellular availability of all-trans retinoic acid in neuroblastoma cells [J].
Armstrong, JL ;
Ruiz, M ;
Boddy, AV ;
Redfern, CPF ;
Pearson, ADJ ;
Veal, GJ .
BRITISH JOURNAL OF CANCER, 2005, 92 (04) :696-704
[9]
Arora R, 2007, ASIAN J PHARM, V1, P29
[10]
Nonionic surfactant vesicles as a carrier for transdermal delivery of frusemide [J].
Azeem, Adnan ;
Ahmad, Farhan Jalees ;
Khan, Zeenat Iqbal ;
Talegaonkar, Sushama .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 2008, 29 (05) :723-730