Abstract

Because of its good biocompatibility and biodegradability, albumins such as bovine serum albumin (BSA) and human serum albumin (HSA) have found a wide range of biomedical applications. Herein, we report that glutaraldehyde cross-linked BSA (or HSA) forms a novel fluorescent biological hydrogel, exhibiting new green and red autofluorescence in vitro and in vivo without the use of any additional fluorescent labels. UV-vis spectra studies, in conjunction with the fluorescence spectra studies including emission, excitation and synchronous scans, indicated that three classes of fluorescent compounds are presumably formed during the gelation process. SEM, FTIR and mechanical tests were further employed to investigate the morphology, the specific chemical structures and the mechanical strength of the as-prepared autofluorescent hydrogel, respectively. Its biocompatibility and biodegradability were also demonstrated through extensive in vitro and in vivo studies. More interestingly, the strong red autofluorescence of the as-prepared hydrogel allows for conveniently and non-invasively tracking and modeling its in vivo degradation based on the time-dependent fluorescent images of mice. A mathematical model was proposed and was in good agreement with the experimental results. The developed facile strategy to prepare novel biocompatible and biodegradable autofluorescent protein hydrogels could significantly expand the scope of protein hydrogels in biomedical applications.

Highlights

  • Because of its good biocompatibility and biodegradability, albumins such as bovine serum albumin (BSA) and human serum albumin (HSA) have found a wide range of biomedical applications

  • Glutaraldehyde predominantly crosslinks ε -amino groups of lysine within BSA13

  • BSA was first dissolved in 0.01 M pH 7.4 PBS buffer solution and glutaraldehyde was added into BSA solution as the cross-linker with the final concentration of 20% BSA and 1% GA

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Summary

Introduction

Because of its good biocompatibility and biodegradability, albumins such as bovine serum albumin (BSA) and human serum albumin (HSA) have found a wide range of biomedical applications. We report that glutaraldehyde cross-linked BSA (or HSA) forms a novel fluorescent biological hydrogel, exhibiting new green and red autofluorescence in vitro and in vivo without the use of any additional fluorescent labels. The strong red autofluorescence of the as-prepared hydrogel allows for conveniently and non-invasively tracking and modeling its in vivo degradation based on the time-dependent fluorescent images of mice. We report a unique glutaraldehyde cross-linked albumin (BSA or HSA) hydrogel which exhibits strong green and red autofluorescence over a large excitation wavelength range. The degradation/diffusion trends predicted by the proposed mathematical model were in good agreement with the time-dependent fluorescence images of mice These results indicate that the newly formed fluorophores in the autofluorescent BSA hydrogel are stable and not degraded after protein degration until they are absorbed into circulation. The developed facile strategy to prepare a unique autofluorescent protein hydrogel could significantly expand the scope of protein hydrogels in biomedical applications

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