Ionic liquid-mediated transcutaneous protein delivery with solid-in-oil nanodispersions

被引:45
作者
Araki, Shota [1 ]
Wakabayashi, Rie [1 ,3 ]
Moniruzzaman, Muhammad [4 ]
Kamiya, Noriho [1 ,2 ,3 ]
Goto, Masahiro [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Dept Appl Chem, Grad Sch Engn, Nishi Ku, Fukuoka 8190395, Japan
[2] Kyushu Univ, Ctr Future Chem, Nishi Ku, Fukuoka 8190395, Japan
[3] Kyushu Univ, Ctr Transdermal Drug Delivery, Nishi Ku, Fukuoka 8190395, Japan
[4] Univ Teknol PETRONAS Bandar Seri Iskandar, Dept Chem Engn, Seri Iskandar 32610, Perak, Malaysia
关键词
ACTIVE PHARMACEUTICAL INGREDIENTS; VACCINE DELIVERY; IMMUNIZATION; SKIN; MICROEMULSION; OPTIMIZATION; PENETRATION; INDUCTION; SOLVENTS; PEPTIDE;
D O I
10.1039/c5md00378d
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
As a potentially safe and non-invasive vaccination method, transcutaneous immunization represents an attractive alternative to conventional vaccine delivery by injection. However, the development of transcutaneous immunization has remained a challenge for a large number of hydrophilic macromolecules including protein and peptide antigens. We report a novel ionic liquid (IL)-mediated transcutaneous vaccine formulation consisting of a solid-in-oil (S/O) nanodispersion of antigen coated with pharmaceutically accepted surfactants dispersed in IL-containing oil. The introduction of the IL [C(12)mim][Tf2N] (1-dodecyl-3-methyl imidazolium bis.trifluoromethyl sulfonyl) amide) as a penetration enhancer in the formulation significantly enhanced the skin permeability of ovalbumin (OVA), a model antigen. It was also found that the IL-mediated S/O nanodispersion obtained high levels of OVA-specific serum IgG compared with both S/O nanodispersions without IL and PBS control. These findings clearly indicate that ILs - which are potentially attractive "green" and "designer" solvents - could serve as potential skin penetration enhancers in transcutaneous vaccination for hydrophilic macromolecules.
引用
收藏
页码:2124 / 2128
页数:5
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