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Preparation of a novel activated carbon microsphere and its in vitro adsorption characteristics for biological molecules 被引量:2
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作者 谢毅妮 高峰 +2 位作者 袁慧慧 梁晓怿 凌立成 《Journal of Chinese Pharmaceutical Sciences》 CAS 2011年第3期302-308,共7页
We prepared a novel pitch-based activated carbon microsphere(ACM)and studied its in vitro adsorption characteristics for biological molecules.The original spherical asphalt particles were prepared through bitumen em... We prepared a novel pitch-based activated carbon microsphere(ACM)and studied its in vitro adsorption characteristics for biological molecules.The original spherical asphalt particles were prepared through bitumen emulsification.After oxidation and burning,ACMs with a range of parameters were prepared.In vitro adsorption experiments of ACMs for biological molecules were carried out.The prepared ACMs possessed a BET specific surface of 1566 m^2/g with a voidage of 0.653 cm^3/g and a volume of micropores of 0.478 cm^3/g.They showed high adsorption for glucose and creatintine.Compared with the medically used carbon powder,the prepared ACMs exhibited significantly lower adsorption for digestion enzymes.In conclusion,the prepared ACMs,as an oral adsorbent candidate,possessed higher BET specific surface area and larger volume of micropores;they also exhibited favorable selective adsorption features for biological molecules. 展开更多
关键词 Activated carbon microsphere Porous structure Adsorption characteristics biological molecules Digestion enzymes
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Interaction between Metal in Metallo Enzyme and Small Biological Molecules 被引量:1
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作者 Hu Jie-Han Shu Zan-Yong +1 位作者 Tao Li-Mei Cheng Guo-Bao(Dalian Institute of Chemical Physics, Academia Sinica, Dalian 116023) 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1996年第1期24-30,共7页
In this work, the existence of interaction between metal in metallo enzyme and small biological molecules such as amino acid in aqueous solution is confirmed for the first time by the experimental data of ESR, NMR,UV-... In this work, the existence of interaction between metal in metallo enzyme and small biological molecules such as amino acid in aqueous solution is confirmed for the first time by the experimental data of ESR, NMR,UV-VIS and enzyme activity. This kind of interaction can affect the enzyme catalytic activity. 展开更多
关键词 biological molecules metallo enzyme INTERACTION
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A review of corneal nerve and limbal stem cell
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作者 Liqun Chen Xianglong Yi 《Eye Science》 2025年第1期68-84,共17页
The cornea is a transparent tissue that serves as the main refractive element of the eye ball.Limbal epithelial stem cells(LESCs),residing in the basal epithelial layer of the Palisades of Vogt located in the corneal ... The cornea is a transparent tissue that serves as the main refractive element of the eye ball.Limbal epithelial stem cells(LESCs),residing in the basal epithelial layer of the Palisades of Vogt located in the corneal limbus between cornea and scleral,are believed to be crucial for the continuous turnover of the corneal epithelium.The proliferation,migration,and differentiation of the LESCs are modulated by unique physical and chemical futures contained within the microenvironment known as the limbal niche.This niche,composed of nerve terminals,cells,extracellular matrix,vasculature,and signaling molecules,is the home for processes such as proliferation,migration and differentiation.Corneal nerve terminals possess special anatomical structures in the limbal region and basal epithelial cells,and they demonstrate pivotal biological effects in the regulation of the LESC function and corneal epithelium homeostasis.Biological molecules such as neuropeptides,neurotransmitters,and neurotrophic factors play a crucial role in modulating the LESCs phenotype responsible for corneal epithelium homeostasis.This paper will review recent studies on how these nerve derived molecules function in this process and provide clear orientations for future research. 展开更多
关键词 CORNEA limbal epithelial stem cells LESCs cornea nerve biological molecules
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Nanotube-Based Chemical and Biomolecular Sensors 被引量:1
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作者 J.Koh B.Kim +2 位作者 S.Hong H.Lim H.C.Choi 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2008年第4期578-588,共11页
We present a brief review about recent results regarding carbon nanotube (CNT)-based chemical and biomolecular sensors. For the fabrication of CNT-based sensors, devices containing CNT channels between two metal ele... We present a brief review about recent results regarding carbon nanotube (CNT)-based chemical and biomolecular sensors. For the fabrication of CNT-based sensors, devices containing CNT channels between two metal electrodes are first fabricated usually via chemical vapor deposition (CVD) process or "surface programmed assembly" method. Then, the CNT surfaces are often functionalized to enhance the selectivity of the sensors. Using this process, highly-sensitive CNT-based sensors can be fabricated for the selective detection of various chemical and biological molecules such as hydrogen, ammonia, carbon monoxide, chlorine gas, DNA, glucose, alcohol, and proteins. 展开更多
关键词 Chemical vapour deposition Carbon nanotubes SENSORS biological molecules Surface programmed assembly
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Synthesis and Crystal Structure of 5-Methoxy- butyrolacto[3,4-b]-1-N-cyclohexylaziridine
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作者 LI Sen-Lan GUO Jin-Bo +1 位作者 YU Zhao-Lian CHEN Qing-Hua 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第8期921-924,共4页
The title compound, 5-methoxy-butyrolacto[3,4-b]-1-N-cyclohexylaziridine 1, has been synthesized via tandem Micheal addition and intramolecular nucleophilic substitution reactions of 5-methoxy-3-bromo-2(5H)-furanone... The title compound, 5-methoxy-butyrolacto[3,4-b]-1-N-cyclohexylaziridine 1, has been synthesized via tandem Micheal addition and intramolecular nucleophilic substitution reactions of 5-methoxy-3-bromo-2(5H)-furanones 4 with primary amines 5, and structurally determined by single-crystal X-ray diffraction. Crystal data: C11H17NO3, Mr = 211.26, monoclinic system, space group P21/c, a = 17.800(3), b = 5.3864(10), c = 12.2571(10)A°, β = 90.449(3)°, V = 1175.1(3) A°^3, Z= 4, De= 1.194 g/cm^3, λ(MoKα) = 0.071073 nm, μ = 0.087 mm^-1 and F(000) = 456. The structure was refined to R = 0.0505 and wR = 0.1208 for 2579 observed reflections (I 〉 2σ(I)). The crystallographic results of molecule 1 show that the functionalized aziridine ring is fused with a lactone ring to form the component with [3.1.0] bicyclic skeleton. 展开更多
关键词 4-methoxybutenolide alkylaziridine biologic active molecule X-ray crystllography
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Synthesis and Crystal Structure of 2,3-Dihydroxymethyl-N-cyclohexylaziridine
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作者 GUO Jin-Bo YU Zhao-Lian +1 位作者 LI Sen-Lan CHEN Qing-Hua 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第8期917-920,共4页
The title compound, 2(S),3(R)-dihydroxymethyl-N-cyclohexylaziridine 1, has been synthesized via tandem Micheal addition and internal nucleophilic substitution reactions of 5-methoxy-3-bromo-2(5H)-furanones 2 wit... The title compound, 2(S),3(R)-dihydroxymethyl-N-cyclohexylaziridine 1, has been synthesized via tandem Micheal addition and internal nucleophilic substitution reactions of 5-methoxy-3-bromo-2(5H)-furanones 2 with cyclohexylamine 3 and subsequent reduction of intermediate 5. Its crystal structure was determined by single-crystal X-ray diffraction. Crystal data:C10H19NO2, Mr = 185.26, monoclinic system, space group P21/n, a = 8.0620(16), b = 7.2013(14), c= 18.555(4) A°, β= 102.30(3)°, V= 1052.5(4)A°^3, Z= 4, De= 1.169 g/cm^3, λ(MoKα) = 0.071073 nm,μ = 0.080 mm^- 1 and F(000) = 408. The structure was refined to R = 0.0439 and wR = 0.1178 for 1839 observed reflections (I 〉 2σ(I)). The crystallographic structure of 1 shows that the functionalized aziridine ring links two hyroxymethyl groups. 展开更多
关键词 2 3-dihydroxymethyl-N-cyclohexylaziridine biologic active molecule X-ray crystallography
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A Valuable Synthetic Route to the Enantiopure Functionalized N-Substituted Aziridines 被引量:6
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作者 李森兰 郭金波 +1 位作者 郁兆莲 陈庆华 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2004年第4期384-389,共6页
Chiral butyrolacto[3,4-b]-2(S)-6(R)-1-N-akylaziridines 7 were synthesized in enantiopure form utilizing racemic 5-methoxy-3-bromo-2(5H)-furanone (5) and available amines (6) as key precursors. After highly effective r... Chiral butyrolacto[3,4-b]-2(S)-6(R)-1-N-akylaziridines 7 were synthesized in enantiopure form utilizing racemic 5-methoxy-3-bromo-2(5H)-furanone (5) and available amines (6) as key precursors. After highly effective reduction of 7, the functionalized 2(S),3(R)-dihyroxymethyl-N-alkylaziridines (8) were obtained in good yields with ≥98% ee. This is a simple and pratical method for the preparation of enantiopure aziridines which are important interme-diates in the synthesis of biologic active molecules. 展开更多
关键词 asymmetric synthesis chiral 2(S) 3(R)-dihyroxymethyl-N-alkylaziridine biologic active molecule X-ray crystllography
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Constructive strategies for drug delivery systems in antivirus disease therapy by biosafety materials
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作者 Li Wang Zhaoshuo Wang +1 位作者 Lingzhi Cao Kun Ge 《Biosafety and Health》 CSCD 2022年第3期161-170,共10页
Due to the coronavirus disease 2019(COVID‐19)pandemic,the development of antiviral drugs has attracted increasing attention.Clinical antiviral drugs show weak solubility,low bioavailability,adverse side effects,or on... Due to the coronavirus disease 2019(COVID‐19)pandemic,the development of antiviral drugs has attracted increasing attention.Clinical antiviral drugs show weak solubility,low bioavailability,adverse side effects,or only limited targets.With the advancement of nanotechnology and material science,biosafety nanomaterials have been constructed for drug delivery systems of antiviral disease therapy,such as liposomes,polymers,gold nanoparticles,and graphene.These nanodrug systems can either deliver synthesized antiviral drugs siRNA/miRNA and small molecular compounds,deliver bioactive large molecular drug proteins and mRNA,or show antiviral activity by themselves.Nanodelivery systems could effectively enhance the efficiency of antiviral drugs by increasing drug loading and host cell uptake with a small size and high specific surface area.This review focused on the biosafety nanomaterials used for antiviral therapy and discussed the options for the design of antiviral drugs in the future. 展开更多
关键词 Antivirus therapy Nanodelivery systems Compound drugs biologically active molecule drugs
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