Novel tretinoin formulations: a drug-in-cyclodextrin-in-liposome approach

被引:36
作者
Ascenso, Andreia [1 ]
Cruz, Mariana [2 ]
Euleterio, Carla [1 ]
Carvalho, Filomena A. [3 ]
Santos, Nuno C. [3 ]
Marques, Helena C. [1 ]
Simoes, Sandra [1 ]
机构
[1] Nanomed & Drug Delivery Syst Grp iMed UL, P-1649003 Lisbon, Portugal
[2] Univ Lisbon, Fac Farm, P-1699 Lisbon, Portugal
[3] Univ Lisbon, Fac Med, Inst Mol Med, Unidade Biomembranas, P-1699 Lisbon, Portugal
关键词
Atomic force microscopy; dimethyl-beta-cyclodextrin; photon correlation spectroscopy/Laser-Doppler anemometry; tretinoin; ultradeformable vesicles; DYNAMIC LIGHT-SCATTERING; ENHANCED SKIN DELIVERY; LIPID VESICLES; ULTRADEFORMABLE VESICLES; CARRIERS; PHOTOSTABILITY; COMPLEXES; RELEASE; TRANSFERSOMES; ISOTRETINOIN;
D O I
10.3109/08982104.2013.788026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: The aims of this experimental work were the incorporation and full characterization of the system Tretinoin-in-dimethyl-beta-cyclodextrin-in-ultradeformable vesicles (Tretinoin-CyD-UDV) and Tretinoin-in-ultradeformable vesicles (Tretinoin-UDV). Methods: The Tretinoin-CyD complex was prepared by kneading and the UDV by adding soybean phosphatidylcholine (SPC) to Tween (R) 80 followed by an appropriate volume of sodium phosphate buffer solution to make a 10%-20% lipid suspension. The resulting suspension was brought to the final mean vesicles size, of approximately 150 nm, by sequential filtration. The physicochemical characterization was based on: the evaluation of mean particle size and polydispersity index (PI) measured by photon correlation spectroscopy (PCS) and atomic force microscopy (AFM) topographic imaging; zeta potential (zeta-potential) and the SPC concentration determined by Laser-Doppler anemometry and an enzymatic-colorimetric test, respectively. The quantification of the incorporated Tretinoin and its chemical stability (during preparation and storage) was assayed by a HPLC at 342 nm. Results: It was possible to obtain the system Tretinoin-CyD-UDV. The mean vesicle size was the most stable parameter during experiments time course. AFM showed that Tretinoin-CyD-UDV samples were very heterogeneous in size, having three distinct subpopulations, while Tretinoin-UDV samples had only one homogeneous size population. The results of the zeta-potential measurements have shown that vesicle surface charge was low, as expected, presenting negative values. The incorporation efficiency was high, and no significant differences between Tretinoin-CyD-UDV and Tretinoin-UDV were observed. However, only Tretinoin-UDV with 20% lipid concentration formulation remained chemically stable during the evaluation period. Conclusion: According to our results, Tretinoin-UDV with 20% lipid concentration seems to be a better approach than Tretinoin-CyD-UDV, attending to the higher chemical stability.
引用
收藏
页码:211 / 219
页数:9
相关论文
共 47 条
[1]  
Ascenso A, 2009, MINI-REV MED CHEM, V9, P1
[2]  
Ascenso A., 2008, FORMULACAO GEL COMPL
[3]   Complexation and Full Characterization of the Tretinoin and Dimethyl-βeta-Cyclodextrin Complex [J].
Ascenso, Andreia ;
Guedes, Rita ;
Bernardino, Raul ;
Diogo, Herminio ;
Carvalho, Filomena A. ;
Santos, Nuno C. ;
Silva, Aida M. ;
Marques, Helena Cabral .
AAPS PHARMSCITECH, 2011, 12 (02) :553-563
[4]  
Becirevic-Lacan M, 1997, STP PHARMA SCI, V7, P343
[5]  
Bharwaj V., 2010, International Journal of Pharmaceutical Sciences and Research, V2, P40
[6]   IMPROVED PARTICLE-SIZE DISTRIBUTION MEASUREMENTS USING MULTIANGLE DYNAMIC LIGHT-SCATTERING [J].
BRYANT, G ;
THOMAS, JC .
LANGMUIR, 1995, 11 (07) :2480-2485
[7]   LIPID VESICLES PENETRATE INTO INTACT SKIN OWING TO THE TRANSDERMAL OSMOTIC GRADIENTS AND HYDRATION FORCE [J].
CEVC, G ;
BLUME, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1104 (01) :226-232
[8]   Lipid vesicles and other colloids as drug carriers on the skin [J].
Cevc, G .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (05) :675-711
[9]   Ultradeformable lipid vesicles can penetrate the skin and other semi-permeable barriers unfragmented.: Evidence from double label CLSM experiments and direct size measurements [J].
Cevc, G ;
Schätzlein, A ;
Richardsen, H .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2002, 1564 (01) :21-30
[10]  
Cevc G, 1997, Expert Opin Investig Drugs, V6, P1887, DOI 10.1517/13543784.6.12.1887