Terpene Composited Lipid Nanoparticles for Enhanced Dermal Delivery of All-trans-Retinoic Acids

被引:42
作者
Charoenputtakun, Ponwanit [1 ]
Pamornpathomkul, Boonnada [1 ]
Opanasopit, Praneet [1 ]
Rojanarata, Theerasak [1 ]
Ngawhirunpat, Tanasait [1 ]
机构
[1] Silpakorn Univ, Fac Pharm, Nakhon Pathom 73000, Thailand
关键词
lipid nanoparticle; terpene; dermal delivery; all-trans-retinoic acid; TRANSDERMAL DRUG-DELIVERY; IN-VITRO; PHYSICOCHEMICAL STABILITY; PERMEATION ENHANCEMENT; PENETRATION ENHANCERS; ASCORBYL PALMITATE; CARRIERS NLC; SKIN; FORMULATION; LIMONENE;
D O I
10.1248/bpb.b14-00015
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
In the present study, terpene composited lipid nanoparticles and lipid nanoparticles were developed and evaluated for dermal delivery of all-trans-retinoic acids (ATRA). Terpene composited lipid nanoparticles and lipid nanoparticles were investigated for size, size distribution, zeta potential, entrapment efficiency, photostability, and cytotoxicity. In vitro skin permeation of ATRA lipid formulations were also evaluated. To explore the ability of lipid nanocarriers to target the skin, the distribution of rhodamine B base in the skin was investigated using confocal laser scanning microscopy (CLSM). The results indicated that the physicochemical characteristics of terpene composited lipid nanoparticles influenced skin permeability. All lipid nanocarriers significantly protected ATRA from photodegradation and were non-toxic to normal human foreskin fibroblast cells in vitro. Solid lipid nanoparticles containing 10% limonene (10% L-SLN) had the highest ATRA skin permeability. Terpene composited SLN and nanostructured lipid carriers (NLC) showed higher epidermal permeation of rhodamine B across the skin based on CLSM image analysis. Our study suggests that terpene composited SLN and NLC can be potentially used as dermal drug delivery carriers for ATRA.
引用
收藏
页码:1139 / 1148
页数:10
相关论文
共 36 条
[1]
Role of novel terpenes in transcutaneous permeation of valsartan: effectiveness and mechanism of action [J].
Ahad, Abdul ;
Aqil, Mohammed ;
Kohli, Kanchan ;
Sultana, Yasmin ;
Mujeeb, Mohd ;
Ali, Asgar .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2011, 37 (05) :583-596
[2]
Baldwin HE, 2013, J DRUGS DERMATOL, V12, P638
[3]
Structure of the skin barrier and its modulation by vesicular formulations [J].
Bouwstra, JA ;
Honeywell-Nguyen, PL ;
Gooris, GS ;
Ponec, M .
PROGRESS IN LIPID RESEARCH, 2003, 42 (01) :1-36
[4]
All-trans retinoic acid-loaded lipid nanoparticles as a transdermal drug delivery carrier [J].
Charoenputtakhun, Ponwanit ;
Opanasopit, Praneet ;
Rojanarata, Theerasak ;
Ngawhirunpat, Tanasait .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2014, 19 (02) :164-172
[5]
Chern WH, 2003, DISSOLUT TECHNOL, P10
[6]
Chinsriwongkul Akhayachatra, 2007, PDA J Pharm Sci Technol, V61, P461
[7]
Essential oils content and antioxidant properties of peel ethanol extract in 18 lemon cultivars [J].
Di Vaio, C. ;
Graziani, G. ;
Gaspari, A. ;
Scaglione, G. ;
Nocerino, S. ;
Ritieni, A. .
SCIENTIA HORTICULTURAE, 2010, 126 (01) :50-55
[8]
Resveratrol-loaded solid lipid nanoparticles versus nanostructured lipid carriers: evaluation of antioxidant potential for dermal applications [J].
Gokce, Evren H. ;
Korkmaz, Emrah ;
Dellera, Eleonora ;
Sandri, Giuseppina ;
Bonferoni, M. Cristina ;
Ozer, Ozgen .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :1841-1850
[9]
Physico-chemical stability of colloidal lipid particles [J].
Heurtault, B ;
Saulnier, P ;
Pech, B ;
Proust, JE ;
Benoit, JP .
BIOMATERIALS, 2003, 24 (23) :4283-4300
[10]
Limonene GP1/PG organogel as a vehicle in transdermal delivery of haloperidol [J].
Lim, PFC ;
Liu, XY ;
Kang, LF ;
Ho, PCL ;
Chan, YW ;
Chan, SY .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 311 (1-2) :157-164