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Drug resistance in leishmaniasis: current drug-delivery systems and future perspectives
被引:0
|作者:
Yasinzai, Masoom
[1
]
Khan, Momin
[1
,2
]
Nadhman, Akhtar
[1
]
Shahnaz, Gul
[3
]
机构:
[1] Quaid I Azam Univ, Fac Biol Sci, Dept Biotechnol, Islamabad, Pakistan
[2] Khyber Med Univ, Inst Basic Med Sci, Dept Microbiol, Peshawar, Pakistan
[3] Quaid I Azam Univ, Fac Biol Sci, Dept Pharm, Islamabad, Pakistan
关键词:
LIPOSOMAL AMPHOTERICIN-B;
SOLID LIPID NANOPARTICLES;
IN-VITRO EVALUATION;
PEDIATRIC VISCERAL LEISHMANIASIS;
CUTANEOUS LEISHMANIASIS;
MULTIDRUG-RESISTANCE;
ANTILEISHMANIAL ACTIVITY;
POLYMERIC NANOPARTICLES;
PENTAVALENT ANTIMONY;
DONOVANI;
D O I:
10.4155/FMC.13.143
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Leishmaniasis is a complex of diseases with numerous clinical manifestations for instance harshness from skin lesions to severe disfigurement and chronic systemic infection in the liver and spleen. So far, the most classical leishmaniasis therapy, despite its documented toxicities, remains pentavalent antimonial compounds. The available therapeutic modalities for leishmaniasis are overwhelmed with resistance to leishmaniasis therapy. Mechanisms of classical drug resistance are often related with the lower drug uptake, increased efflux, the faster drug metabolism, drug target modifications and over-expression of drug transporters. The high prevalence of leishmaniasis and the appearance of resistance to classical drugs reveal the demand to develop and explore novel, less toxic, low cost and more promising therapeutic modalities. The review describes the mechanisms of classical drug resistance and potential drug targets in Leishmania infection. Moreover, current drug-delivery systems and future perspectives towards Leishmaniasis treatment are also covered.
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页码:1877 / 1888
页数:12
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