目的：制备可生物降解的卡铂白蛋白微球。
OBJECTIVE: To prepare biodegradable albumin microspheres containing carboplatin.
目的优化八氟丙烷白蛋白微球混悬液的制备工艺。
OBJECTIVE To optimize preparation of encapsulated octafluoropropane albumin microspheres.
目的运用灰色数学理论预测长效缓释蛋白微球的体外释药过程。
OBJECTIVE To predict drug release from the extended formulations by grey maths model.
方法以醋酸乙酯为油相，采用乳化化学交联技术制备白蛋白微球。
METHODS ADM-AMS were prepared by emulsion-chemical cross linking technique, using ethyl acetate as oil phase.
目的：测定心脏超声造影剂声微显注射液的白蛋白微球浓度和直径。
OBJECTIVES:To analyse air-filled albumin microspheres of Shengweixian injection, an ultrasound contrast agent.
目的探讨全氟丙烷白蛋白微球注射剂左心超声造影临床应用的可行性。
AIM: To evaluate the feasibility of clinical application of left heart contrast echocardiography with perfluoropropane-albumin microsphere.
探索茶多酚磁性白蛋白微球的制备工艺，用作治疗肿瘤的新型动脉栓塞制剂。
To explore the method of preparing tea polyphenols magnetic albumin microspheres, which are used to a new arterial embolization formulation.
用乳化化学交联法制备出适合于颌面部鳞癌殒外动脉栓塞用顺铂白蛋白微球；
In this paper the technique of emulsion chemical-crosslinking was used to prepare cisplatin albumin microsphere for jaw squamous cancer by neck external artery embolization.
目的：比较米托蒽醌白蛋白微球和联糖米托蒽醌白蛋白微球肝靶向性的优劣。
OBJECTIVE: To study the liver targeting effect of DHAQ BSA MS and Gal DHAQ BSA MS.
该蛋白微球新剂型改善了载药微球悬浮液的稳定性，抑制了释药初期的突释现象。
Zein microsphere tablets improved the stability of the zein microsphere enclosed drugs in suspension and suppressed the phenomenon of sudden release at the first stage of delivery.
目的：考察热固化时间及温度对喷雾干燥牛血清白蛋白微球表面活性氨基含量的影响。
OBJECTIVE: Effects of heat denaturation time duration and temperature on the surface reactive amino group content of spray dried bovine serum albumin microspheres were investigated.
目的优化阿昔洛韦白蛋白微球的制备工艺，并对其形态学性质、载药量、体外释药进行考察。
OBJECTIVE To study the preparation of aciclovir loaded albumin microspheres (ACV BSA MS) and evaluate its morphology, drug loading and release in vitro.
方法氟尿嘧啶包封于白蛋白微球，并经小鼠尾静脉给药后，采用HPLC离子抑制技术，测定氟尿嘧啶在小鼠血浆、心、肝、肺、肾、脾、脑中的浓度。
METHOD After intravenous injection in mice, the concentrations of 5 fluorouracil in mice plasma, heart, liver, lung, kidney, spleen and brain were determined respectively by HPLC.
采用磁性壳聚糖微球吸附的方法吸附大豆乳清废水中蛋白质。
Adsorption effects of magnetic chitosan microsphere on protein of soy whey waste water were studied in this paper.
实验结果表明，纤维素磁性微球作为性能优良的新型磁性载体，更适于目的蛋白的免疫磁性分离。
The result suggested that MCMS were much more suitable for purification of aim proteins than other microspheres and showed an extensive application foreground for immunomagnetic separation.
目的考察活性保护剂对微球中蛋白活性的保护作用。
OBJECTIVE to investigate the effect of activity protectors on the protein activity in microspheres.
结论两亲磁性高分子微球可作为分离人血清白蛋白的有效手段。
CONCLUSION Amphiphilic magnetic polymer microspheres were an effective means for the separation of HSA.
实验观察到微球与基片表面的结合力受到配基面密度的影响，说明发生结合的是多对而非单对蛋白质分子。
It was found that the adhesion force between the spheres and the chip surface was affected by the ligand surface concentration.
因此，自70年代以来，磁性微球作为一种新型的功能材料，在细胞分离、蛋白质提纯、免疫测定和靶向药物等诸多领域有着广阔的应用前景。
Therefore, since 1970's, as a new type of functional material, it has gained broad applications in cell separation, protein purification, immunoassays, immobilized enzyme and target delivery of drug.
观察了自制丝裂霉素C（MMC）白蛋白磁性微球用于裸鼠人肝癌模型的疗效。
The effects of ferromagnetic protein MMC bearing microsphere (FMS) were observed on human liver cancer model in nude mice.
然后，以壳聚糖微球为载体，用吸附-交联的联合固定化方法制备固定化木瓜蛋白酶，并研究了木瓜蛋白酶的最佳固定化条件。
Then as the carrier, the chitosan microspheres were used to immobilize papain by absorption crosslinking method. The optimum conditions for immobilization were studied.
本文的目的是制备交联海藻酸钠磁性微球，并用于固定化胰蛋白酶。
The aim of this paper is to prepare magnetic particle of crosslinked Alginate Sodium and to apply it to immobilize Trypsin.
方法根据国内外文献，较全面地总结了PLGA微球中稳定蛋白，解决不完全释放的策略。
METHODS On the base of literatures at home and abroad, strategies to improve the stability of protein and facilitate its complete release were generally summarized here.
结论：以琼脂凝胶微球载体，通过交联、活化和固定配基色氨酸成功制备免疫球蛋白e免疫吸附剂。
CONCLUSION: IgE immunoadsorbent is successfully prepared through cross-linking, activation of AGAR gel beads and immobilization of tryptophan ligand.
结果与结论多肽、蛋白质药物缓释微球在药学领域有着广阔的发展前景。
Results and Conclusions Polypeptide-protein microspheres have broad prospects in the pharmaceutical filed.
复乳法是制备蛋白质药物plga微球最常用的方法。
The double emulsion method is the often used technique for preparation of protein drugs loaded PLGA microspheres.
本研究为鸡球虫微线蛋白结构与功能研究提供了依据和实验材料，为进一步研制基因工程疫苗提供了候选抗原。
This study can be used for understanding of structure and function of microneme proteins and development of genetically modified vaccine.
该嵌段共聚物微球能提高蛋白、多肽的稳定性，有利于难溶性药物释放。
The microspheres of PEG-PLA block copolymers can enhance the stability of protein and polypeptide, and profit the release of poorly water-soluble pharmaceuticals.
将20种光谱自编码微球与20种不同物种的免疫球蛋白和血清样品一一对映包被，然后将其全部混合在一起，进行多样品混合ELISA筛选。
Twenty samples are coated on 20 different optical self-encoding microbeads respectively. All beads were mixed after coating and washing for multi-samples ELISA mix-screening.
将20种光谱自编码微球与20种不同物种的免疫球蛋白和血清样品一一对映包被，然后将其全部混合在一起，进行多样品混合ELISA筛选。
Twenty samples are coated on 20 different optical self-encoding microbeads respectively. All beads were mixed after coating and washing for multi-samples ELISA mix-screening.
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