Structure and Morphology Changes during in Vitro Degradation of Electrospun Poly(glycolide-co-lactide) Nanofiber Membrane

• Published in: Biomacromolecules 2003-03, Vol.4 (2), p.416-423
• Main Authors: Zong, Xinhua, Ran, Shaofeng, Kim, Kwang-Sok, Fang, Dufei, Hsiao, Benjamin S, Chu, Benjamin
• Format: Article
• Language: English
• Subjects: Applied sciences; Calorimetry, Differential Scanning; Exact sciences and technology; Exchange resins and membranes; Forms of application and semi-finished materials; In Vitro Techniques; Lactic Acid - chemistry; Membranes, Artificial; Polyglycolic Acid - chemistry; Polymer industry, paints, wood; Polymers - chemistry; Technology of polymers; X-Ray Diffraction
• ISSN: 1525-7797; 1526-4602
• DOI: 10.1021/bm025717o

Electrospun poly(glycolide-co-lactide) (PLA10GA90, LA/GA ratio 10/90) biodegradable nanofiber membranes possessed very high surface area to volume ratios and were completely noncrystalline with a relatively lowered glass transition temperature. These characteristics led to very different structure, morphology, and property changes during in vitro degradation, which were examined systematically. A shrinkage study showed that the electrospun crystallizable but amorphous PLA10GA90 membranes exhibited a very small shrinkage percentage when compared with the electrospun membranes of noncrystallizable poly(lactide-co-glycolide) (PLA75GA25, LA/GA 75/25) and poly(d,l-lactide). Although the weight loss of electrospun PLA10GA90 membranes exhibited a similar degradation behavior as cast thin films, detailed studies showed that the structure and morphology changes in electrospun membranes followed different pathways during the hydrolytic degradation. After 1 day of degradation in buffer solution at 37 °C, electrospun PLA10GA90 membranes exhibited a sudden increase in crystallinity and glass transition temperature, due to the fast thermally induced crystallization process. The continuous increase in crystallinity and apparent crystal size, as well as the decrease in long period and lamellae thickness, indicated that the thermally induced crystallization was followed by a chain cleavage induced crystallization process. The mass loss rate was accelerated after 6 days of degradation. The increase in glass transition temperature during this period further confirmed that the degradation of PLA10GA90 nanofibers was initiated from the amorphous region within the lamellar superstructures. A mechanism of structure and morphology changes during in vitro degradation of electrospun PLA10GA90 nanofibers is proposed.