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Merck

430471

Sigma-Aldrich

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

ester terminated, Mw 50,000-75,000

Sinónimos:

Lactel® B6006-1, PLGA

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1 G
68,20 €
5 G
236,00 €

68,20 €


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1 G
68,20 €
5 G
236,00 €

About This Item

Fórmula lineal:
[C3H4O2]x[C2H2O2]y
Número MDL:
Código UNSPSC:
12162002
ID de la sustancia en PubChem:
NACRES:
NA.23

68,20 €


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Nivel de calidad

Formulario

amorphous

cociente alimentación

lactide:glycolide 85:15

mol peso

Mw 50,000-75,000

marco temporal de la degradación

<6 months

viscosidad

0.55-0.75 dL/g, 0.1 % (w/v) in chloroform(25 °C)

temperatura de transición

Tg 45-50 °C

solubilidad

ethyl acetate, chloroform, acetone and THF: soluble

temp. de almacenamiento

2-8°C

cadena SMILES

OCC(O)=O.CC(O)C(O)=O

InChI

1S/C3H6O3.C2H4O3/c1-2(4)3(5)6;3-1-2(4)5/h2,4H,1H3,(H,5,6);3H,1H2,(H,4,5)

Clave InChI

XBBVURRQGJPTHH-UHFFFAOYSA-N

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Descripción general

Characteristic properties of ester terminated poly(D,L-lactide-co-glycolide) (PLGA) are in vivo biodegradability, tunable drug release profile and very high encapsulation capacity.[1]

Aplicación

PLGA polymers find uses in the production of biodegradable medical sutures and for controlled drug release. PLGA microspheres have been reported for use in controlled release of human growth hormone.[1] Thin membranes of blended polymers constituting of PLGA/polycaprolactone/β-tricalcium phosphate have been used in guided bone regeneration.[2]

Características y beneficios

Controlled release of bioactive agents, sutures and bioabsorbable implantable devices.

Forma física

Biocompatible, biodegradable polymer.

Información legal

Lactel is a registered trademark of Evonik Corp

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Certificados de análisis (COA)

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Fabrication of blended polycaprolactone/poly (lactic-co-glycolic acid)/?-tricalcium phosphate thin membrane using solid freeform fabrication technology for guided bone regeneration
Shim JH, et al.
Tissue Engineering: Part A, 19(3-4), 317-328 null
Preparation and characterization of poly (D, L-lactide-co-glycolide) microspheres for controlled release of human growth hormone
Capan Y, et al.
Aaps Pharmscitech, 4(2), 147-156 (2003)
Manjae Gil et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 5(6), 1800024-1800024 (2018-06-26)
Anisotropically compartmentalized microparticles have attracted increasing interest in areas ranging from sensing, drug delivery, and catalysis to microactuators. Herein, a facile method is reported for the preparation of helically decorated microbuilding blocks, using a modified electrohydrodynamic cojetting method. Bicompartmental microfibers
Ayelen L Helling et al.
Tissue engineering. Part A, 25(3-4), 214-223 (2018-10-04)
In human skin the junction between the epidermis and dermis undulates. Epidermal stem cells pattern according to their position relative to those undulations. Here we describe a rig in which epidermal cells are cultured on a collagen-coated poly(d,l-lactide-co-glycolide) (PLGA) membrane.
Teresa Musumeci et al.
International journal of pharmaceutics, 440(2), 135-140 (2012-10-20)
Melatonin, a neurohormone secreted by the pineal gland, is able to modulate intraocular pressure (IOP). The aim of this study was to generate nanoparticle (NPs) sustained release formulations that allow to extend the pre-corneal residence time of melatonin, thus prolonging

Artículos

Interest in utilizing biodegradable polymers for biomedical applications has grown since the 1960s.

Synthetic aliphatic polyesters dominate resorbable biomaterials in clinical use.

AliAliphatic polyesters, including polylactide and polyglycolide, are biodegradable polymers widely used in medical applications.

Immunosuppressive tumor-associated myeloid cells (TAMC) are responsible for glioblastoma (GBM) resistance to immunotherapies and existing standard of care treatments. This mini-review highlights recent progress in implementing nanotechnology in advancing TAMC-targeted therapies for GBM.

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Preguntas

1–6 de 6 Preguntas  
  1. What are the end groups of Product No. 430471 (Poly(DL-lactide-co-glycolide)?

    1 respuesta
    1. Product 430471 has a dodecyl (12 carbon) ester on one end of the polymer chain and a hydroxyl end group on the other.

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  2. What is the tensile strength of Product No. 403471 Poly(DL-lactide-co-glycolide)?

    1 respuesta
    1. Product 430471 has a tensile strength of 6000 - 8000 psi, with an elongation of 3-10%.

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  3. What is the Department of Transportation shipping information for this product?

    1 respuesta
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  4. What is the density of Product No. 430471 Poly(DL-lactide-co-glycolide)?

    1 respuesta
    1. According to the manufacturer, product 430471 has a theoretical density of 1.27g/mL.

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  5. Is Product No. 403471 a resorbable polymer?

    1 respuesta
    1. Yes, Product No. 430471 has a resorption time of 5-6 months.

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  6. How is this Product No. 430471 synthesized (Poly(DL-lactide-co-glycolide)?

    1 respuesta
    1. To synthesize product 430471, 1-dodecanol is used as an initiator and stannous octoate is used as a catalyst to start the ring opening polymerization of D,L-lactide and glycolide monomers.

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