Mingzhong Li

Structure and properties of silk fibroin-poly(vinyl alcohol) gel

A series of porous silk fibroin-poly(vinyl alcohol) blend gels were prepared from corresponding aqueous mixtures by freeze- or air-drying, and their structure and mechanical properties were examined. The air-dried gels had higher crystallinity and much greater strengths than the freeze-dried gels, and therefore are suitable for mechanical uses. The freeze-dried gels had characteristic porous structure potentially useful as cell culture substrate. Its structure could be systematically varied by changing freezing temperature and freeze-thaw pretreatments before drying.

Compliant film of regenerated Antheraea pernyi silk fibroin by chemical crosslinking

A compliant film was prepared by chemical crosslinking of fibroin from silk fiber of wild silkworm, Antheraea pernyi. The silk fiber was dissolved in concentrated aqueous lithium thiocyanate and desalinated by dialysis. The film was cast from the regenerated aqueous solution, and crosslinked by polyethylene glycol diglycidyl ether (PEG-DE). This film showed high water resistively while maintaining random coil and alpha-helix structure, unlike films prepared by organic solvent treatment that causes beta-sheet formation. The films containing about 20wt.% crosslinker were remarkably compliant and tenacious. These features, combined with the living-cell affinity of the wild silkworm fibroin, are expected to be useful in biomedical applications.

Ion-induced fabrication of silk fibroin nanoparticles from Chinese oak tasar Antheraea pernyi

Silk protein fibroin in nanoparticles form is a promising material for drug delivery due to its pleiotropic properties, including biocompatibility, biodegradability, ease in fabrication into smaller diameters, high bioavailability, and therapeutic retention at target sites. In the present study, silk nanoparticles are fabricated from regenerated fibroin solution of the Chinese temperate oak tasar Antheraea pernyi by novel ion-induced self-assembly in a very short time under mild conditions. The resultant fibroin nanoparticles range in size from 100 to 500 nm. The molecular conformation of regenerated fibroin changes from α-helical to a β-sheet structure as a rapid function of the ionic strength and the hydrophobic and electrostatic interactions. The mild conditions are potentially advantageous for the encapsulation of sensitive drugs and therapeutic molecules such as doxorubicin hydrochloride, an amphiphilic anticancer therapeutic. In vitro release of doxorubicin from nanoparticles is pH sensitive, with approx. 65% doxorubicin remaining in the fibroin nanoparticles after 11 days. The activity of fibroin nanoparticles on hepatomas indicates the efficacy of the fibroin nanoparticles to maintain the bioactivity of the loaded doxorubicin and impart a dose-dependent cell growth inhibition. The results suggest that Chinese temperate oak tasar silk fibroin nanoparticles can be used as a sustained drug delivery vehicle.

Soft freezing-induced self-assembly of silk fibroin for tunable gelation

Silk fibroin (SF) hydrogel is a promising candidate in biomaterial field; however its application is quite limited by long-gelation time. In the present study, we developed a novel strategy named soft freezing to accelerate the process and control the sol-gel transition of SF protein. SF protein was induced to self-assembly by soft freezing process for achieving the reconstructed SF solution with metastable structure. It was found that the soft freezing process triggers the structural transition from random structure to ordered structure-rich conformation. Gelation kinetics showed that the gelation time of SF protein could be regulated by changing freezing time and initial concentration. The reconstructed SF solution allowed enhanced sol-gel transition within 6 hours, even at extremely low concentration. The attractive features of the method described here include the accelerated gelation, free of chemical agents, and reducing processing complexity. The SF solution with short gelation time will be applicable as cell encapsulation and injectable applications for tissue engineering and regenerative medicine, which greatly expand the applications of SF hydrogels.

Facile preparation of bioactive silk fibroin/hyaluronic acid hydrogels

Proteins and polysaccharides are primary components in mammal soft tissue. In this study, we established a rapid hydrogel to imitate the nature extracellular matrix via silk fibroin (SF) and hyaluronic acid (HA) blend hydrogel. SF/HA hydrogel was prepared effectively, and its formation time was shorted. With the increase of HA content, the water absorption, porosity and breaking strengths of the hydrogel increased, while hydrophilic of the hydrogel was enhanced extremely determined by contact angle decreasing. Especially, the SF/HA hydrogel with a ratio of 5:5 presented the highest water absorption and mechanical properties. The molecule conformation of the composite hydrogel was mainly amorphous structure and contained the small number of β-sheets which gradually decreases with the increase of HA content. In drug release test, accumulative release ratio of the composite gel was about 80% at day 40. And the mass loss of the hydrogel reached approximately 78% in vitro degradation. In vivo, the SF/HA hydrogels presented good histocompatibility and promoted vascular-like tissue regeneration when were implanted subcutaneously of Sprague Dawley rats. This study provides a new approach to fabricate silk-based biomaterials for soft tissue regeneration.