9-Nitrocamptothecin (9-NC) is an orally administered topoisomerase-I inhibitor for the treatment of pancreatic carcinoma, but its oral absorption and bioavailability are poor. The main objective of this study was to develop optimal 9-nitrocamptothecin (9-NC) microemulsion prepared by self-microemulsifying drug delivery system (SMEDDS). Two SMEDDS formulations of 9-NC prepared from a mixture of ethyl oleate, Tween-80 (T-form) or Cremophor EL (C-form), and PEG-400/ethanol were formed as microemulsions under dilution with aqueous phase. The resulting microemulsions were evaluated in vitro and in vivo, including the kinetics and antitumor effects in SKOV-3 human ovarian cancer xenograft in nude mice. Following 1:10 aqueous dilution of optimal 9...
BACKGROUND: Hepatocellular carcinoma (HCC) is the third most common cause of cancer related mortalit...
Many hydrophobic cancer drugs such as docetaxel (DTX) and etoposide (ETP) have been widely used as c...
The main purpose of this study was to investigate the potential of self-nano-emulsifying drug delive...
9-Nitrocamptothecin (9-NC) is an orally administered topoisomerase-I inhibitor for the treatment of ...
This study explored the design of supersaturable self-microemulsifying drug delivery systems (S-SMED...
The aim of the study was to develop a novel oil/water microemulsion system to increase the cytotoxic...
Multidrug resistance (MDR) is the major underlying cause of the low 5-year survival rate of esophage...
目的 制备9-硝基喜树碱(9-NC)自微乳化静脉注射给药系统,并考察其在大鼠体内的药动学情况.方法 采用伪三元相图确定微乳形成的区域,以正交实验方法确定最佳处方,并对9-NC自微乳化制剂的稳定性进行了...
Purpose: Irinotecan (CPT-11) and SN-38 - its active metabolite - are alkaloid-derived topoisomerase ...
In recent years, combining different types of therapy has emerged as an advanced strategy for cancer...
Purpose: Irinotecan (CPT-11) and SN-38 - its active metabolite - are alkaloid-derived topoisomerase ...
Ana Casadó,1,2 M Lluïsa Sagristá,1 Margarita Mora1 1Department of Biochemistry a...
In order to tackle the problems on low water solubility of teniposide, involvement of toxic surfacta...
The objective of the present investigation was to formulate self-microemulsifying drug delivery syst...
Approximately 70-75% of medications marketed worldwide are administrated per os and are proven to be...
BACKGROUND: Hepatocellular carcinoma (HCC) is the third most common cause of cancer related mortalit...
Many hydrophobic cancer drugs such as docetaxel (DTX) and etoposide (ETP) have been widely used as c...
The main purpose of this study was to investigate the potential of self-nano-emulsifying drug delive...
9-Nitrocamptothecin (9-NC) is an orally administered topoisomerase-I inhibitor for the treatment of ...
This study explored the design of supersaturable self-microemulsifying drug delivery systems (S-SMED...
The aim of the study was to develop a novel oil/water microemulsion system to increase the cytotoxic...
Multidrug resistance (MDR) is the major underlying cause of the low 5-year survival rate of esophage...
目的 制备9-硝基喜树碱(9-NC)自微乳化静脉注射给药系统,并考察其在大鼠体内的药动学情况.方法 采用伪三元相图确定微乳形成的区域,以正交实验方法确定最佳处方,并对9-NC自微乳化制剂的稳定性进行了...
Purpose: Irinotecan (CPT-11) and SN-38 - its active metabolite - are alkaloid-derived topoisomerase ...
In recent years, combining different types of therapy has emerged as an advanced strategy for cancer...
Purpose: Irinotecan (CPT-11) and SN-38 - its active metabolite - are alkaloid-derived topoisomerase ...
Ana Casadó,1,2 M Lluïsa Sagristá,1 Margarita Mora1 1Department of Biochemistry a...
In order to tackle the problems on low water solubility of teniposide, involvement of toxic surfacta...
The objective of the present investigation was to formulate self-microemulsifying drug delivery syst...
Approximately 70-75% of medications marketed worldwide are administrated per os and are proven to be...
BACKGROUND: Hepatocellular carcinoma (HCC) is the third most common cause of cancer related mortalit...
Many hydrophobic cancer drugs such as docetaxel (DTX) and etoposide (ETP) have been widely used as c...
The main purpose of this study was to investigate the potential of self-nano-emulsifying drug delive...