Preparation of a solid-in-oil nanosuspension containing L-ascorbic acid as a novel long-term stable topical formulation

被引:26
作者
Piao, Hongyu [2 ]
Kamiya, Noriho [1 ,3 ]
Cui, Fude [2 ]
Goto, Masahiro [1 ,3 ]
机构
[1] Grad Sch Engn, Dept Appl Chem, Tokyo, Japan
[2] Shenyang Pharmaceut Univ, Dept Pharmaceut, Coll Pharm, Shenyang 110016, Peoples R China
[3] Kyushu Univ, Ctr Future Chem, Fukuoka 8190395, Japan
关键词
L-Ascorbic acid; Topical formulation; Solid-in-oil nanosuspension; Stabilization; Enzymatic degradation; Mixture surfactant systems; VITAMIN-C; ORAL DELIVERY; DEGRADATION; VITRO; ANTIOXIDANTS; SKIN;
D O I
10.1016/j.ijpharm.2011.08.025
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
L-Ascorbic acid (AA, vitamin C) easily decomposes into inactive compounds in aqueous solutions and this has limited its topical use. This work reports the preparation of a solid-in-oil nanosuspension (SONS) containing AA and validation of its basic storage stability. Although AA itself is water-soluble, it can readily be nanosuspended in squalane via complex formation involving a combination of sucrose erucate (i.e. lipophilic surfactant) and sucrose monolaureate (i.e. hydrophilic surfactant) to yield SONS with a very low moisture content (<500 ppm). To extract encapsulated AA, a lipase-based enzymatic degradation technique was used to degrade a formulation phase making it easier for AA to distribute into an extraction solution. Our results demonstrate that almost all the encapsulated AA (95.3%) was readily extracted from the SONS upon addition of medium-chain triglyceride, which offers the possibility of degrading the formulation phase using lipase. Finally, its storage stability study was investigated at 25 degrees C over 90 days under protection from light. An aqueous solution containing AA was used as a control. Compared with the control, the SONS markedly increased the stability of AA due to its low moisture content and, thus, the potential usefulness SONSs as a novel long-term stable topical formulation of AA has been proved. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 160
页数:5
相关论文
共 25 条
[1]
BISSETT DL, 1990, PHOTODERMATOL PHOTO, V7, P56
[2]
BODE AM, 1990, CLIN CHEM, V36, P1807
[3]
TOPICAL VITAMIN-C PROTECTS PORCINE SKIN FROM ULTRAVIOLET RADIATION-INDUCED DAMAGE [J].
DARR, D ;
COMBS, S ;
DUNSTON, S ;
MANNING, T ;
PINNELL, S .
BRITISH JOURNAL OF DERMATOLOGY, 1992, 127 (03) :247-253
[4]
DAVIS SS, 1981, CHEM IND, V19, P670
[5]
Formulation and evaluation of a vitamin C multiple emulsion [J].
Farahmand, S. ;
Tajerzadeh, H. ;
Farboud, E. S. .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2006, 11 (02) :255-261
[6]
On the stability of ascorbic acid in emulsified systems for topical and cosmetic use [J].
Gallarate, M ;
Carlotti, ME ;
Trotta, M ;
Bovo, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 188 (02) :233-241
[7]
Inhibitory effect of magnesium L-ascorbyl-2-phosphate (VC-PMG) on melanogenesis in vitro and in vivo [J].
Kameyama, K ;
Sakai, C ;
Kondoh, S ;
Yonemoto, K ;
Nishiyama, S ;
Tagawa, M ;
Murata, T ;
Ohnuma, T ;
Quigley, J ;
Dorsky, A ;
Bucks, D ;
Sagamihara, KB .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 34 (01) :29-33
[8]
Effect of colloidal carriers on ascorbyl palmitate stability [J].
Kristl, J ;
Volk, B ;
Gasperlin, M ;
Sentjurc, M ;
Jurkovic, P .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 19 (04) :181-189
[9]
UV photoprotection by combination topical antioxidants vitamin C and vitamin E [J].
Lin, JY ;
Selim, MA ;
Shea, CR ;
Grichnik, JM ;
Omar, MM ;
Monteiro-Riviere, NA ;
Pinnell, SR .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2003, 48 (06) :866-874
[10]
REGULATION OF COLLAGEN-SYNTHESIS BY ASCORBIC-ACID [J].
MURAD, S ;
GROVE, D ;
LINDBERG, KA ;
REYNOLDS, G ;
SIVARAJAH, A ;
PINNELL, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (05) :2879-2882