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Key Documents

808482

Sigma-Aldrich

Poly(D,L-lactide-co-glycolide)

lactide:glycolide 50:50, acid and hydroxy terminated, Mn 25000

Synonym(s):

HO-PLGA-COOH, PLGA, heterobifunctional PLGA

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About This Item

Linear Formula:
HO(C3H4O2)x(C2H2O2)yH
UNSPSC Code:
12162002

form

crystals

mol wt

Mn 25000

storage temp.

2-8°C

Application

Heterobifunctional degradable PLGA for conjugation, grafting and functionalization for drug delivery applications.[1][2]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Saurabh Srivastava et al.
Journal of cancer research and therapeutics, 15(3), 480-490 (2019-06-07)
The aim of the study to develop surface modified targeted moiety α-tocopherol (α-t) encapsulated with 5-fluorouracil (5-FU)-poly-D, L-lactic-co-glycolic acid nanoparticles (PLGA NPs) toward the anticancer activity against oral squamous cell carcinoma (OSCC). 5-FU was conjugated with the polymer, PLGA by
Kun Wei et al.
International journal of pharmaceutics, 464(1-2), 225-233 (2014-01-28)
Di-block polymer of poly (lactic-co-glycolic acid)-poly (ethylene glycol) (PLGA-PEG) end-capped with capecitabine (CAP) at the hydrophobic domain and folate (FA) at hydrophilic domain were synthesized respectively. The products were extensively studied by nuclear magnetic resonance ((1)H NMR) and gel permeation
Grafting of telechelic poly(lactic-co-glycolic acid) onto O2 plasma-treated polypropylene flakes.
Ren J, et al.
Journal of Applied Polymer Science, 121, 210-216 (2011)

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