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Sigma-Aldrich

Polyglycolic acid

Synonym(s):

PGA, Poly(2-hydroxyacetic acid)

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About This Item

CAS Number:
26009-03-0
MDL number:
MFCD00148011
UNSPSC Code:
12162002
PubChem Substance ID:
24870413

description

inherent viscosity 1.2 dl/g

InChI

1S/C2H4O3/c3-1-2(4)5/h3H,1H2,(H,4,5)

InChI key

AEMRFAOFKBGASW-UHFFFAOYSA-N

Application

medical device

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Hongfen Wei et al.
PloS one, 8(3), e58133-e58133 (2013-03-08)
The distribution of targeted nanoparticles in tumor tissue is affected by a combination of various factors such as the physicochemical properties of the nanoparticles, tumor hemoperfusion and tumor vascular permeability. In this study, the impact of the biological effects of
Elias A Rivera et al.
Methods in molecular biology (Clifton, N.J.), 1001, 353-374 (2013-03-16)
The accurate interpretation of histological outcomes is a critical endpoint in preclinical studies. Thus, the toxicologic pathologist plays a vital role in conducting a comprehensive microscopic evaluation that would ultimately help defining the safety and functionality in Tissue Engineering/Regenerative Medicinal
Qingxing Xu et al.
Biomaterials, 34(15), 3902-3911 (2013-03-05)
The drug release and degradation behavior of two double-walled microsphere formulations consisting of a doxorubicin-loaded poly(d,l-lactic-co-glycolic acid) (PLGA) core (∼46 kDa) surrounded by a poly(d,l-lactic acid) (PDLLA) shell layer (∼55 and 116 kDa) were examined. It was postulated that different molecular weights
Richard G Payne et al.
Methods in molecular biology (Clifton, N.J.), 1001, 167-177 (2013-03-16)
This chapter describes the fabrication of a polyglycolic acid (PGA)-based scaffold used to tissue engineer a Neo-Urinary Conduit™.
Huaping Chen et al.
Biomaterials, 34(16), 4159-4172 (2013-03-14)
The absence of safe, efficient, cost-effective, and easily scalable delivery platforms is one of the most significant hurdles and critical issues that limit the bench to bedside translation of oligonucleotides-based therapeutics. Acid-labile materials are of special interest in developing nonviral
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