Kamdem Tamo Arnaud, Doench Ingo, Morales Helguera Aliuska, Hoenders Daniel, Walther Andreas, Madrazo Anayancy Osorio
Institute of Microsystems Engineering IMTEK, Laboratory for Sensors, University of Freiburg, 79110 Freiburg, Germany.
Freiburg Materials Research Center FMF, University of Freiburg, 79104 Freiburg, Germany.
Polymers (Basel). 2020 Jul 9;12(7):1522. doi: 10.3390/polym12071522.
Recent advances in nanocellulose technology have revealed the potential of crystalline cellulose nanofibers to reinforce materials which are useful for tissue engineering, among other functions. However, the low biodegradability of nanocellulose can possess some problems in biomedical applications. In this work, alginate particles with encapsulated enzyme cellulase extracted from were prepared for the biodegradation of crystalline cellulose nanofibers, which carrier system could be incorporated in tissue engineering biomaterials to degrade the crystalline cellulose nanoreinforcement in situ and on-demand during tissue regeneration. Both alginate beads and microparticles were processed by extrusion-dropping and inkjet-based methods, respectively. Processing parameters like the alginate concentration, concentration of ionic crosslinker Ca, hardening time, and ionic strength of the medium were varied. The hydrolytic activity of the free and encapsulated enzyme was evaluated for unmodified (CNFs) and TEMPO-oxidized cellulose nanofibers (TOCNFs) in suspension (heterogeneous conditions); in comparison to solubilized cellulose derivatives (homogeneous conditions). The enzymatic activity was evaluated for temperatures between 25-75 °C, pH range from 3.5 to 8.0 and incubation times until 21 d. Encapsulated cellulase in general displayed higher activity compared to the free enzyme over wider temperature and pH ranges and for longer incubation times. A statistical design allowed optimizing the processing parameters for the preparation of enzyme-encapsulated alginate particles presenting the highest enzymatic activity and sphericity. The statistical analysis yielded the optimum particles characteristics and properties by using a formulation of 2% (w/v) alginate, a coagulation bath of 0.2 M CaCl and a hardening time of 1 h. In homogeneous conditions the highest catalytic activity was obtained at 55 °C and pH 4.8. These temperature and pH values were considered to study the biodegradation of the crystalline cellulose nanofibers in suspension. The encapsulated cellulase preserved its activity for several weeks over that of the free enzyme, which latter considerably decreased and practically showed deactivation after just 10 d. The alginate microparticles with their high surface area-to-volume ratio effectively allowed the controlled release of the encapsulated enzyme and thereby the sustained hydrolysis of the cellulose nanofibers. The relative activity of cellulase encapsulated in the microparticles leveled-off at around 60% after one day and practically remained at that value for three weeks.
纳米纤维素技术的最新进展揭示了结晶纤维素纳米纤维在增强材料方面的潜力,这些材料可用于组织工程以及其他功能。然而,纳米纤维素的低生物降解性在生物医学应用中可能会带来一些问题。在这项工作中,制备了包封有从[具体来源未给出]提取的纤维素酶的藻酸盐颗粒,用于结晶纤维素纳米纤维的生物降解,该载体系统可被整合到组织工程生物材料中,以便在组织再生过程中原位且按需降解结晶纤维素纳米增强材料。藻酸盐珠粒和微粒分别通过挤出滴加法和基于喷墨的方法制备。改变了诸如藻酸盐浓度、离子交联剂Ca的浓度、硬化时间和介质的离子强度等加工参数。在悬浮液(非均相条件)中,针对未改性的(CNFs)和TEMPO氧化的纤维素纳米纤维(TOCNFs)评估了游离酶和包封酶的水解活性;并与溶解的纤维素衍生物(均相条件)进行了比较。在25 - 75°C的温度、3.5至8.0的pH范围内以及长达21天的孵育时间下评估了酶活性。在更宽的温度和pH范围内以及更长的孵育时间内,包封的纤维素酶总体上比游离酶表现出更高的活性。通过统计设计优化了制备具有最高酶活性和球形度的酶包封藻酸盐颗粒的加工参数。统计分析得出,使用2%(w/v)藻酸盐、0.2 M CaCl₂的凝固浴和1小时的硬化时间的配方可得到最佳颗粒特性和性能。在均相条件下,在55°C和pH 4.8时获得了最高催化活性。考虑这些温度和pH值来研究悬浮液中结晶纤维素纳米纤维的生物降解。包封的纤维素酶比游离酶的活性多保持了几周,后者在仅仅10天后就大幅下降并几乎失活。具有高表面积与体积比的藻酸盐微粒有效地实现了包封酶的控释,从而实现了纤维素纳米纤维的持续水解。微粒中包封的纤维素酶的相对活性在一天后稳定在约60%,并在三周内基本保持该值。