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Merck
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文件

67122

Sigma-Aldrich

Poly(D-lactide)

inherent viscosity ~1.2 dl/g

别名:

D-Lactide polymer

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About This Item

CAS号:
106989-11-1
MDL號碼:
MFCD00131929
分類程式碼代碼:
12352209
PubChem物質ID:
24885094
NACRES:
NA.25

分子量

Mn ~90000
Mp ~95000
Mw ~124000

儲存溫度

2-8°C

SMILES 字串

CC(O)C(O)=O

應用

Poly(D-lactide) (PDLA), a polymer of a stereospecific cyclic di-ester of lactic acid, is used in biomaterial research for the development of devices such as therapeutic drug delivery vessels. Poly(D-lactide) is used for the preparation of microparticles and resorbable polylactide scaffolds.

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

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Jun Shao et al.
The journal of physical chemistry. B, 116(33), 9983-9991 (2012-08-02)
Stereocomplex poly(lactide)s (sc-PLAs) were obtained from solution blending of 3-armed poly(L-lactide) (3PLLA) and linear poly(D-lactide) (PDLA) and between enantiomeric 3PLAs. Differential scanning calorimetry and wide-angle X-ray diffraction results indicated that racemic crystallites were preferentially produced in all the binary blends.
Jingru Sun et al.
The journal of physical chemistry. B, 115(12), 2864-2869 (2011-03-10)
The effects of the addition of poly(D-lactide) (PDLA) on the crystallization behavior of poly(L-lactide)(PLLA) were investigated by means of differential scanning calorimetry (DSC) and temperature-dependent X-ray diffraction(XRD). When the blends were cooled from different temperatures (250, 240, and 190 °C)
J R Sarasua et al.
Journal of materials science. Materials in medicine, 22(11), 2513-2523 (2011-08-23)
Bioresorbable polylactides are one of the most important materials for tissue engineering applications. In this work we have prepared scaffolds based on the two optically pure stereoisomers: poly(L: -lactide) (PLLA) and poly(D: -lactide) (PDLA). The crystalline structure and morphology were
Jamal S Lewis et al.
Biomaterials, 33(29), 7221-7232 (2012-07-17)
Microparticulate systems for delivery of therapeutics to DCs for immunotherapy have gained attention recently. However, reports addressing the optimization of DC-targeting microparticle delivery systems are limited, particularly for cases where the goal is to deliver payload to DCs in a

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