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BP11140 PLGA 65:35, Hydroxyl Terminated, IV: 0.08–0.18 dl/g, Mw: 5–15 kDa

Catalogue Number BP11140
Composition Poly(D, L-lactide-co-glycolide) 65:35, Hydroxyl Terminated
Form Powder

PLGA 65:35, Hydroxyl Terminated, IV: 0.08–0.18 dl/g, Mw: 5–15 kDa is a biodegradable copolymer synthesised from lactic and glycolic acids with a 65:35 ratio. Stanford Advanced Materials (SAM) produces this material using controlled polymerisation techniques and systematic molecular weight monitoring. A standardised gel permeation chromatography process confirms the inherent viscosity range, ensuring batch-to-batch consistency and predictable degradation behaviour for biomedical applications.

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

What advantages does hydroxyl termination provide in this PLGA copolymer?

Hydroxyl termination enables further chemical modifications and enhances chain-end reactivity. This facilitates conjugation with active molecules, which can be valuable in drug delivery or tissue engineering where surface functionalisation is critical for performance.

How does the inherent viscosity range of 0.08–0.18 dl/g influence its application?

The inherent viscosity range correlates directly with the polymer’s molecular weight and degradation rate. A lower viscosity typically indicates shorter polymer chains, leading to faster hydrolytic breakdown, which is beneficial in applications requiring controlled resorption rates.

What processing considerations are important when using PLGA in powder form?

When processing PLGA powder, it is important to control moisture and temperature to prevent premature degradation. Uniform particle distribution and proper mixing techniques are essential to ensure consistent performance in formulations, particularly in drug delivery systems.

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