Biodegradable injectable in situ depot-forming drug delivery systems

被引:75
作者
Chitkara, Deepak
Shikanov, Ariella
Kumar, Neeraj
Domb, Abraham J.
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Pharmaceut, SAS Nagar 160062, Mohali, India
[2] Hebrew Univ Jerusalem, Dept Med Chem & Nat Prod, IL-91120 Jerusalem, Israel
关键词
biodegradable; drug delivery systems; in situ crosslinked systems; in situ precipitation; thermally induced gelling systems; thermoplastic pastes;
D O I
10.1002/mabi.200600129
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The scope of drug-delivery systems has expanded significantly in recent years providing new ways to deliver life saving therapeutics to patients. The development of new injectable drug-delivery systems has provided new vistas and opened up unexplored horizons in the field of science, particularly in controlled drug delivery since these systems possess unique advantages over traditional ones, which include ease of application, and localized and prolonged drug delivery. In the past few years, an increasing number of such systems has been reported in the literature for various biomedical applications, including drug delivery, cell encapsulation, and tissue repair. These are injectable fluids that can be introduced into the body in a minimally invasive manner prior to solidifying or gelling within the desired site. For this purpose both natural (chitosan, alginates) as well as synthetic polymers (PEGylated polyesters, ricinoleic acid-based polymers) have been utilized. These systems have been explored widely for the delivery of various therapeutic agents ranging for anti-neoplastic agents like 1 paclitaxel to proteins and peptides such as insulin, almost covering every segment of the pharmaceutical field. This manuscript focuses on the recent advancements in the area of in situ forming biodegradable polymeric drug-delivery systems.
引用
收藏
页码:977 / 990
页数:14
相关论文
共 67 条
[1]   Development of biodegradable injectable thermoplastic oligomers [J].
Amsden, B ;
Hatefi, A ;
Knight, D ;
Bravo-Grimaldo, E .
BIOMACROMOLECULES, 2004, 5 (02) :637-642
[2]   In vivo degradation behavior of photo-cross-linked star-poly(ε-caprolactone-co-D,L-lactide) elastomers [J].
Amsden, BG ;
Tse, MY ;
Turner, ND ;
Knight, DK ;
Pang, SC .
BIOMACROMOLECULES, 2006, 7 (01) :365-372
[3]   Regional radiochemotherapy using in situ hydrogel [J].
Azhdarinia, A ;
Yang, DJ ;
Yu, DF ;
Mendez, R ;
Oh, C ;
Kohanim, S ;
Bryant, J ;
Kim, EE .
PHARMACEUTICAL RESEARCH, 2005, 22 (05) :776-783
[4]   Thermogelling poly(caprolactone-b-ethylene glycol-b-caprolactone) aqueous solutions [J].
Bae, SJ ;
Suh, JM ;
Sohn, YS ;
Bae, YH ;
Kim, SW ;
Jeong, B .
MACROMOLECULES, 2005, 38 (12) :5260-5265
[5]   Self-cross-linking biopolymers as injectable in situ forming biodegradable scaffolds [J].
Balakrishnan, B ;
Jayakrishnan, A .
BIOMATERIALS, 2005, 26 (18) :3941-3951
[6]   A novel non-toxic camptothecin formulation for cancer chemotherapy [J].
Berrada, M ;
Serreqi, A ;
Dabbarh, F ;
Owusu, A ;
Gupta, A ;
Lehnert, S .
BIOMATERIALS, 2005, 26 (14) :2115-2120
[7]   PEG-grafted chitosan as an injectable thermosensitive hydrogel for sustained protein release [J].
Bhattarai, N ;
Ramay, HR ;
Gunn, J ;
Matsen, FA ;
Zhang, MQ .
JOURNAL OF CONTROLLED RELEASE, 2005, 103 (03) :609-624
[8]   Phase inversion dynamics of PLGA solutions related to drug delivery - Part II. The role of solution thermodynamics and bath-side mass transfer [J].
Brodbeck, KJ ;
DesNoyer, JR ;
McHugh, AJ .
JOURNAL OF CONTROLLED RELEASE, 1999, 62 (03) :333-344
[9]   Thermosensitive behavior of poly(ethylene oxide)-poly[bis(methoxyethoxyethoxy)phosphazenel block copolymers [J].
Chang, YK ;
Powell, ES ;
Allcock, HR ;
Park, SM ;
Kim, C .
MACROMOLECULES, 2003, 36 (07) :2568-2570
[10]   Controlled delivery of testosterone from smart polymer solution based systems: In vitro evaluation [J].
Chen, SB ;
Singh, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 295 (1-2) :183-190