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BP11128 PLGA 65:35, Lauryl Ester Terminated, IV: 1.0–2.0 dl/g, Mw: 158–410 kDa

Catalogue Number BP11128
Composition Poly(D, L-lactide-co-glycolide) 65:35, Lauryl Ester Terminated
Form Powder

PLGA 65:35, Lauryl Ester Terminated is a functionalised biodegradable copolymer with a lactide-to-glycolide molar ratio of 65:35. The incorporation of lauryl ester end groups enhances the polymer's hydrophobicity and effectively modulates its degradation kinetics, making it particularly suitable for sustained-release formulations and hydrophobic drug delivery systems.

Stanford Advanced Materials (SAM) employs controlled synthesis processes and rigorous quality assurance systems, supported by spectroscopic and chromatographic characterisation methods. Intrinsic viscosity is determined using Ubbelohde capillary viscometry, providing key insights into polymer chain length and solution behaviour. Each batch undergoes validated analytical testing to ensure structural consistency, functional reliability, and compliance with specifications for advanced biomedical research and product development.

In addition to the standard 65:35 grade, SAM offers customised synthesis of PLGA copolymers with various lactide-to-glycolide ratios, such as 90:10, 85:15, 80:20, 70:30, 65:35, and 60:40. We also provide tailored molecular weights, end-group modifications, and physical forms to meet diverse application requirements.

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FAQ

How does the lauryl ester termination affect the degradation rate of the PLGA copolymer?

The lauryl ester termination moderates the hydrolytic degradation of the polymer by reducing water uptake at the polymer chain end. This controlled degradation is critical in applications where predictable drug release kinetics and structural integrity over time are required.

What processing techniques are recommended for PLGA 65:35 applications in biomedical devices?

Solvent casting and melt extrusion are commonly used processing techniques for this PLGA type. These methods preserve the polymer's molecular structure and ensure uniform dispersion when integrated into composite matrices for biomedical devices.

Can the polymer’s intrinsic viscosity range be correlated to its performance in drug delivery systems?

Yes, the intrinsic viscosity range of 1.0–2.0 dl/g is indicative of controlled chain length and molecular weight distribution, which directly impacts drug release rates. This parameter assists in tailoring the polymer matrix for specific release profiles in therapeutic applications.

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