Development and Characterization of Thiolated Cyclodextrin-Based Nanoparticles for Topical Delivery of Minoxidil

被引:3
作者
Akhtar, Ammara [1 ]
Waqas, Muhammad Khurram [1 ]
Mahmood, Arshad [2 ,3 ]
Tanvir, Saira [4 ]
Hussain, Talib [1 ]
Kazi, Mohsin [5 ]
Ijaz, Muhammad [6 ,7 ]
Asim, Mulazim Hussain [8 ]
机构
[1] UVAS, Inst Pharmaceut Sci, Lahore 54000, Pakistan
[2] Al Ain Univ, Coll Pharm, Abu Dhabi Campus,POB 112612, Abu Dhabi, U Arab Emirates
[3] Al Ain Univ, AAU Hlth & Biomed Res Ctr HBRC, POB 112612, Abu Dhabi, U Arab Emirates
[4] Ripha Int Univ, Riphah Inst Pharmaceut Sci, Islamabad 44000, Pakistan
[5] King Saud Univ, Coll Pharm, Dept Pharmaceut, POB 2457, Riyadh 11451, Saudi Arabia
[6] Univ Coll Dublin, Sch Vet Med, Dublin D04 C1P1, Ireland
[7] COMSATS Univ Islamabad, Dept Pharm, Lahore Campus,Def Rd,1-5 Km Raiwind Rd, Lahore 54000, Pakistan
[8] Univ Sargodha, Coll Pharm, Sargodha 40100, Pakistan
关键词
thiomers; cyclodextrin; hair keratin; minoxidil; hair adhesion; SOLID LIPID NANOPARTICLES; BETA-CYCLODEXTRIN; INCLUSION COMPLEX; IN-VITRO; HAIR-GROWTH; SYSTEM;
D O I
10.3390/pharmaceutics15122716
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: The aim of this research was to prepare adhesive nanoparticles for the topical application of Minoxidil (MXD). Methods: Thiolated beta-CDs were prepared via conjugation of cysteamine with oxidized CDs. MXD was encapsulated within thiolated and unmodified beta-CDs. Ionic gelation method was used to prepare nanoparticles (Thio-NP and blank NP) of CDs with chitosan. Nanoparticles were analyzed for size and zetapotential. Inclusion complexes were characterized via FTIR. Drug dissolution studies were carried out. An in vitro adhesion study over human hair was performed. An in vivo skin irritation study was performed. Ex vivo drug uptake was evaluated by using a Franz diffusion cell. Results: Thiolated beta-CDs presented 1804.68 +/- 25 mu mol/g thiol groups and 902.34 +/- 25 mu mol/g disulfide bonds. Nanoparticles displayed particle sizes within a range of 231 +/- 07 nm to 354 +/- 13 nm. The zeta potential was in the range of -8.1 +/- 02 mV, +16.0 +/- 05 mV. FTIR analyses confirmed no interaction between the excipients and drug. Delayed drug release was observed from Thio-NP. Thio-NP retained over hair surfaces for a significantly longer time. Similarly, drug retention was significantly improved. Thio-NP displayed no irritation over rabbit skin. Conclusion: Owing to the above results, nanoparticles developed with MXD-loaded thiolated beta-CDs might be a potential drug delivery system for topical scalp diseases.
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页数:14
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