Cinnamic acid derived compounds loaded into liposomes: antileishmanial activity, production standardisation and characterisation

被引:8
作者
Campos Cury, Thuanny Alexandra [1 ]
Yoneda, Juliana Sakamoto [1 ]
Zuliani, Juliana Pavan [2 ,3 ]
Soares, Andreimar Martins [4 ]
Stabeli, Rodrigo Guerino [5 ]
Calderon, Leonardo de Azevedo [4 ,6 ]
Ciancaglini, Pietro [1 ]
机构
[1] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Quim, BR-14040901 Sao Paulo, Brazil
[2] Univ Fed Rondonia UNIR, Fundacao Oswaldo Cruz Fiocruz, Lab Imunol Celular Aplicada Saude, Fiocruz Rondonia, Porto Velho, Rondonia, Brazil
[3] Univ Fed Rondonia UNIR, Dept Med, Porto Velho, Rondonia, Brazil
[4] Fundacao Oswaldo Cruz Fiocruz, Ctr Estudos Biomol Aplicadas Saude, Fiocruz Rondonia, Porto Velho, Rondonia, Brazil
[5] Ctr Nanotecnol Aplicada Saude Nanosus, Presidencia Fiocruz, Curitiba, Parana, Brazil
[6] Univ Fed Rondonia UNIR, Dept Med, Porto Velho, Rondonia, Brazil
基金
巴西圣保罗研究基金会;
关键词
Antileishmanial activity; drug carrier; Leishmaniasis; liposomes; Leishmania amazonensis; PIPER-TUBERCULATUM JACQ; LEISHMANIA-AMAZONENSIS; MEGLUMINE ANTIMONIATE; IN-VITRO; PHOSPHATIDYLCHOLINE; MACROPHAGE; DIVERSITY; SPP;
D O I
10.3109/02652048.2015.1046518
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Synthetic compounds derived from cinnamic acid were tested in cultures containing the promastigote form of Leishmania amazonensis and the dimethylsulphoxide solution of B2 compound (2.0 mg/mL) led to a 92% decrease of leishmania in 96 h of treatment. Then, different liposomal systems (diameters similar to 200 nm) were prepared by the extrusion method in the presence and absence of compounds studied. DSC thermograms of the liposomes in the presence of these compounds caused changes in Delta H, T-m and Delta T-1/2, compared to controls, indicating that there was an interaction of the compounds with the lipid bilayer. Assays with negatively charged liposomal systems containing these drugs in L. amazonensis cultures led to a 50-80% decrease in the number of leishmanias with a concentration to 100 times lower when compared to the B2 initial test. These liposomal systems are promoting more interaction and delivery of the compounds and proved to be an efficient, stable and promising system.
引用
收藏
页码:467 / 477
页数:11
相关论文
共 42 条
[31]   Association of acylated cationic decapeptides with dipalmitoylphosphatidylserine-dipalmitoyl- phosphatidylcholine lipid membranes [J].
Pedersen, TB ;
Sabra, MC ;
Frokjaer, S ;
Mouritsen, OG ;
Jorgensen, K .
CHEMISTRY AND PHYSICS OF LIPIDS, 2001, 113 (1-2) :83-95
[32]   Leishmania and the macrophage: a multifaceted interaction [J].
Podinovskaia, Maria ;
Descoteaux, Albert .
FUTURE MICROBIOLOGY, 2015, 10 (01) :111-129
[33]   An ethanolic extract of leaves of Piper betle (Paan) Linn mediates its antileishmanial activity via apoptosis [J].
Sarkar, Avijit ;
Sen, Rupashree ;
Saha, Piu ;
Ganguly, Sudipto ;
Mandal, Goutam ;
Chatterjee, Mitali .
PARASITOLOGY RESEARCH, 2008, 102 (06) :1249-1255
[34]   Characterization of DODAB/DPPC vesicles [J].
Sobral, Cecilia N. C. ;
Soto, Marco A. ;
Carmona-Ribeiro, Ana M. .
CHEMISTRY AND PHYSICS OF LIPIDS, 2008, 152 (01) :38-45
[35]   A Review of Preventative Methods against Human Leishmaniasis Infection [J].
Stockdale, Lisa ;
Newton, Robert .
PLOS NEGLECTED TROPICAL DISEASES, 2013, 7 (06)
[36]   Antitrypanosomal and antileishmanial activities of flavonoids and their analogues:: In vitro, in vivo, structure-activity relationship, and quantitative structure-activity relationship studies [J].
Tasdemir, D ;
Kaiser, M ;
Brun, R ;
Yardley, V ;
Schmidt, TJ ;
Tosun, F ;
Rüedi, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (04) :1352-1364
[37]   Targeting Leishmania (L.) chagasi amastigotes through macrophage scavenger receptors:: the use of drugs entrapped in liposomes containing phosphatidylserine [J].
Tempone, AG ;
Perez, D ;
Rath, S ;
Vilarinho, AL ;
Mortara, RA ;
de Andrade, HF .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 54 (01) :60-68
[38]   Lysophosphatidylcholine exacerbates Leishmania major-dendritic cell infection through interleukin-10 and a burst in arginase1 and indoleamine 2,3-dioxygenase activities [J].
Tounsi, Nabila ;
Meghari, Soraya ;
Moser, Muriel ;
Djerdjouri, Bahia .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2015, 25 (01) :1-9
[39]   Physicochemical characterization and cytotoxic studies of nonionic surfactant vesicles using sucrose esters as oral delivery systems [J].
Valdes, Karina ;
Morilla, Maria Jose ;
Romero, Eder ;
Chavez, Jorge .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2014, 117 :1-6
[40]  
Velazquez-Campoy Adrian, 2004, Curr Protoc Cell Biol, VChapter 17, DOI 10.1002/0471143030.cb1708s23