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Protein Adsorption onto Nanosized Hydroxyapatite Particles for Controlled Drug Release 被引量:1

Protein Adsorption onto Nanosized Hydroxyapatite Particles for Controlled Drug Release
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摘要 Nanosized hydroxyapatite(nsHAp) was synthesized to examine its possibility as a controlled release cartier of protein. To achieve effective protein release from nanosized hydroxyapatite, the study of the adsorptive properties of protein on nsHAp and different influence parameters such as pH, calcium, and phosphate concentrations during the adsorption process is necessary. Ovalbumin(OVA) was selected as the model of growth factors. The results show that the amount of OVA adsorbed onto nsHAp in acetic buffer(pH = 3.6) is more than that in acetic buffer(pH =5.6) because of the electric interaction. The amount of OVA adsorption in phosphate buffer solution(PBS) is smaller than that in acetic buffer because of surface complexation and surface hydroxylation. The presence of Ca^2+ dramatically increases the adsorbed amount of OVA in acetic buffer on maintaining the same pH. Meanwhile, the release kinetics of OVA adsorbed onto nsHAp(nsHAp-OVA) was also examined. The amount of released OVA in PBS(pH = 5.6) was significantly smaller than that released in solution of pH = 7.0. All the results suggest that nanosized hydroxyapatite particles could be successfully used as controlled released carrier of protein. Nanosized hydroxyapatite(nsHAp) was synthesized to examine its possibility as a controlled release cartier of protein. To achieve effective protein release from nanosized hydroxyapatite, the study of the adsorptive properties of protein on nsHAp and different influence parameters such as pH, calcium, and phosphate concentrations during the adsorption process is necessary. Ovalbumin(OVA) was selected as the model of growth factors. The results show that the amount of OVA adsorbed onto nsHAp in acetic buffer(pH = 3.6) is more than that in acetic buffer(pH =5.6) because of the electric interaction. The amount of OVA adsorption in phosphate buffer solution(PBS) is smaller than that in acetic buffer because of surface complexation and surface hydroxylation. The presence of Ca^2+ dramatically increases the adsorbed amount of OVA in acetic buffer on maintaining the same pH. Meanwhile, the release kinetics of OVA adsorbed onto nsHAp(nsHAp-OVA) was also examined. The amount of released OVA in PBS(pH = 5.6) was significantly smaller than that released in solution of pH = 7.0. All the results suggest that nanosized hydroxyapatite particles could be successfully used as controlled released carrier of protein.
出处 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2007年第3期254-257,共4页 高等学校化学研究(英文版)
基金 Supported by Graduate Innovation Lab of Jilin University, P R China
关键词 NANOMATERIALS HYDROXYAPATITE OVALBUMIN Controlled release Nanomaterials Hydroxyapatite Ovalbumin Controlled release
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