2004
DOI: 10.1002/jps.20100
|View full text |Cite
|
Sign up to set email alerts
|

Development of solid lipid nanoparticles containing ionically complexed chemotherapeutic drugs and chemosensitizers

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
104
0
1

Year Published

2008
2008
2016
2016

Publication Types

Select...
7
1

Relationship

2
6

Authors

Journals

citations
Cited by 154 publications
(108 citation statements)
references
References 34 publications
1
104
0
1
Order By: Relevance
“…[1,3] Since then, various PLN formulations have been developed to encapsulate a single anticancer drug, [4] or co-encapsulate a drug with a chemosensitizer, [1,3] a drug with a P-glycoprotein (P-gp) inhibitor, [5] or dual anticancer drugs of synergy. [6] PLN formulations have also been developed to deliver biologics for gene therapy and immunotherapy, including siRNA [7] or siRNA with an anticancer drug.…”
Section: Emergence and Progress Of Pln Developmentmentioning
confidence: 99%
See 1 more Smart Citation
“…[1,3] Since then, various PLN formulations have been developed to encapsulate a single anticancer drug, [4] or co-encapsulate a drug with a chemosensitizer, [1,3] a drug with a P-glycoprotein (P-gp) inhibitor, [5] or dual anticancer drugs of synergy. [6] PLN formulations have also been developed to deliver biologics for gene therapy and immunotherapy, including siRNA [7] or siRNA with an anticancer drug.…”
Section: Emergence and Progress Of Pln Developmentmentioning
confidence: 99%
“…endogenous fatty acids). Up to date, reported PLN formulations can be divided into two major categories as schematically illustrated in Figure 1: type A -monolithic matrix PLN, where polymer and drug(s) are homogeneously distributed in the solid lipid matrix, [1,[3][4][5][6][9][10][11][12] and type Bcore-shell PLN, where drug-containing polymer core is covered by a single layer of phospholipid. [7,8,13] The latter is sometimes called lipid-polymer hybrid nanoparticles (LPN) in literature.…”
Section: Composition and Design Of Plnmentioning
confidence: 99%
“…Afterward, the mixture was further treated by sonication (90 W) for 15 min at 75 °C. The emulsion was poured into cold water (2 -4 °C) to a final volume of 25 ml [10], and then the suspension was passed through a homogenizer (Emulsiflex-c3, Avestin, Canada) for five cycles (30 s for each cycle) at 20,000 bars. Particle size determination…”
Section: Preparation Of Clindamycin-loaded Slnsmentioning
confidence: 99%
“…SLNs are usually applicable for entrapping lipophilic drugs [9,10]. However, for loading highly water-soluble, ionic drugs such as clindamycin, SLN formulations face the challenge of low drug partitioning in the lipid phase [11].…”
Section: Introductionmentioning
confidence: 99%
“…However, these studies also showed that SLNs delivered reduced amount of drugs into Serpe, 2006;Ying, 2008;Wong, 2004Wong, , 2006aWong, , 2006bCavalli, 1993 Han, 2008ibuprofen Casadei, 2006Paolicelli, 2008idarubicin Cavalli, 1993insulin Battaglia, 2007Bi, 2009;Gallarate, 2008;Liu 2008,a,d,;Sarmento, 2007magnetite Hsu, 2008methotrexate Paliwal, 2008Ruckmani, 2006mitoxanthrone Lu, 2006nimesulide Bondi, 2009nitrendipine Bhaskar, 2009bKumar, 2007;Manjunath, 2006olanzapine Vivek, 2007oridonin Zhang, 2005oxymatrine Sun, 2007paclitaxel Dong, 2008Lee, 2007;Cavali, 2000;Stevens, 2004;Serpe, 2004;Chen, 2001 (2010) heart, lung, spleen, liver and kidney (Zara et al, 2000;Fundaro et al, 2000;, which suggest that biodistribution of drugs in SLNs can vary depending on the composition of SLNs.…”
Section: Biodistributionmentioning
confidence: 99%