Macrophage specific drug delivery in experimental leishmaniasis

被引:55
作者
Basu, MK [1 ]
Lala, S [1 ]
机构
[1] Indian Inst Chem Biol, Biomembrane Div, Kolkata 700032, W Bengal, India
关键词
D O I
10.2174/1566524043360186
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Macrophage-specific delivery systems are the subject of much interest nowadays, because of the fact that macrophages act as host cells for many parasites and bacteria, which give rise to outbreak of so many deadly diseases(eg. leishmaniasis, tuberculosis etc.) in humans. To combat these deadly diseases initially macrophage specific liposomal delivery system were thought of and tested in vivo against experimental leishmaniasis in hamsters using a series of indigenous or synthetic antileishmanial compounds and the results were critically discussed. In vitro testing was also done against macrophages infected with Leishmania donovani, the causative agent for visceral leishmaniasis. The common problem of liposome therapy being their larger size, stability and storage, non-ionic surfactant vesicles, niosomes were prepared, for their different drug distribution and release characteristics compared to liposomes. When tested in vivo, the retention capacity of niosomes was found to be higher than that of liposomes due to the absence of lipid molecules and their smaller size. Thus the therapeutic efficacy of certain antileishmanial compounds was found to be better than that in the liposomal form. The niosomes, being cheaper, less toxic, biodegradable and non-immunogenic, were considered for sometime as suitable alternatives to liposomes as drug carriers. Besides the advent of other classical drugs carriers(e.g. neoglycoproteins), the biggest challenge came from polymeric delivery vehicles, specially the polymeric nanoparticles which were made of cost effective biodegradable polymers and different natural polymers. Because of very small size and highly stable nature, use of nanoparticles as effective drug carriers has been explored in experimental leishmaniasis using a series of antileishmanial compounds, both of indigenous and synthetic origin. The feasibility of application in vivo, when tested for biological as well as for other physicochemical parameters, the polymeric nanoparticles have turned out to be the best and thus may be projected for effective use in the clinics.
引用
收藏
页码:681 / 689
页数:9
相关论文
共 67 条
[1]   SYNERGISTIC EFFECT OF GLUCANTIME AND A LIPOSOME-ENCAPSULATED MURAMYL DIPEPTIDE ANALOG IN THERAPY OF EXPERIMENTAL VISCERAL LEISHMANIASIS [J].
ADINOLFI, LE ;
BONVENTRE, PF ;
VANDERPAS, M ;
EPPSTEIN, DA .
INFECTION AND IMMUNITY, 1985, 48 (02) :409-416
[2]  
Afrin F, 2000, J PARASITOL, V86, P730, DOI 10.1645/0022-3395(2000)086[0730:IOPPAL]2.0.CO
[3]  
2
[4]   Characterization of Leishmania donovani antigens encapsulated in liposomes that induce protective immunity in BALB/c mice [J].
Afrin, F ;
Rajesh, R ;
Anam, K ;
Gopinath, M ;
Pal, S ;
Ali, N .
INFECTION AND IMMUNITY, 2002, 70 (12) :6697-6706
[5]   Superior chemotherapeutic efficacy of amphotericin B in tuftsin-bearing liposomes against Leishmania donovani infection in hamsters [J].
Agrawal, AK ;
Agrawal, A ;
Pal, A ;
Guru, PY ;
Gupta, CM .
JOURNAL OF DRUG TARGETING, 2002, 10 (01) :41-45
[6]   TISSUE DISTRIBUTION AND ANTILEISHMANIAL ACTIVITY OF LIPOSOMISED AMPHOTERICIN-B IN BALB/C MICE [J].
AHMAD, I ;
AGARWAL, A ;
PAL, A ;
GURU, PY ;
BACHHAWAT, BK ;
GUPTA, CM .
JOURNAL OF BIOSCIENCES, 1991, 16 (04) :217-221
[7]  
Alving C. R., 1982, Targeting of drugs. (NATO Advanced Study Institutes Series A, Vol. 47)., P337
[8]   THERAPY OF LEISHMANIASIS - SUPERIOR EFFICACIES OF LIPOSOME-ENCAPSULATED DRUGS [J].
ALVING, CR ;
STECK, EA ;
CHAPMAN, WL ;
WAITS, VB ;
HENDRICKS, LD ;
SWARTZ, GM ;
HANSON, WL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (06) :2959-2963
[9]   LIPOSOMES IN LEISHMANIASIS - THERAPEUTIC EFFECTS OF ANTIMONIAL DRUGS, 8-AMINOQUINOLINES, AND TETRACYCLINE [J].
ALVING, CR ;
STECK, EA ;
CHAPMAN, WL ;
WAITS, VB ;
HENDRICKS, LD ;
SWARTZ, GM ;
HANSON, WL .
LIFE SCIENCES, 1980, 26 (26) :2231-2238
[10]   DELIVERY OF LIPOSOME-ENCAPSULATED DRUGS TO MACROPHAGES [J].
ALVING, CR .
PHARMACOLOGY & THERAPEUTICS, 1983, 22 (03) :407-424