有机-无机复合骨修复材料

本文对近5年来有机/无机复合骨修复材料研究领域的进展进行了综述,根据材料组分的特点分析其在生物相容性、生物降解性、生物活性以及力学性能等方面的优缺点,同时探讨了目前骨修复材料领域存在的问题,并对今后人工骨替代材料的发展趋势作出了展望。     

丝素纤维/硫酸钙抗感染骨材料的制备及性能

通过控制丝素蛋白自组装过程制备了溶液状态下的丝素纳米纤维（silk fibroin nanofibers,SFFs）,与硫酸钙、万古霉素（vancomycin,VCM）复合,制备了VCM/CS/SFFs抗菌骨材料。通过SEM、XRD、紫外分光光度计、万能力学试验机、抑菌圈、MTT等手段分别研究了复合材料的微观形貌与结构、药物释放、力学、抑菌及细胞相容性等性能。结果显示,与水作为固化液相比,随着SFFs溶液（0.017 5~2.1 mg·mL^-1）的加入,复合材料凝固时间可控,降解率逐渐降低,抗水性增强,韧性提高;同时随丝素纳米纤维含量的增加骨材料抗压强度表现为先增加后减小的趋势,一周内药物释放速率降低;材料同时具有抑菌作用;MTT实验结果显示,加入丝素纳米纤维后与纯的硫酸钙相比MC3T3细胞增殖明显。     

Applications of Vibrational Spectroscopy for Analysis of Connective Tissues

Advances in vibrational spectroscopy have propelled new insights into the molecular composition and structure of biological tissues. In this review, we discuss common modalities and techniques of vibrational spectroscopy, and present key examples to illustrate how they have been applied to enrich the assessment of connective tissues. In particular, we focus on applications of Fourier transform infrared (FTIR), near infrared (NIR) and Raman spectroscopy to assess cartilage and bone properties. We present strengths and limitations of each approach and discuss how the combination of spectrometers with microscopes (hyperspectral imaging) and fiber optic probes have greatly advanced their biomedical applications. We show how these modalities may be used to evaluate virtually any type of sample (ex vivo, in situ or in vivo) and how “spectral fingerprints” can be interpreted to quantify outcomes related to tissue composition and quality. We highlight the unparalleled advantage of vibrational spectroscopy as a label-free and often nondestructive approach to assess properties of the extracellular matrix (ECM) associated with normal, developing, aging, pathological and treated tissues. We believe this review will assist readers not only in better understanding applications of FTIR, NIR and Raman spectroscopy, but also in implementing these approaches for their own research projects.     

丝素纤维/硫酸钙抗感染骨材料的制备及性能

通过控制丝素蛋白自组装过程制备了溶液状态下的丝素纳米纤维(silk fibroin nanofibers,SFFs),与硫酸钙、万古霉素(vancomycin,VCM)复合,制备了VCM/CS/SFFs抗菌骨材料。通过SEM、XRD、紫外分光光度计、万能力学试验机、抑菌圈、MTT等手段分别研究了复合材料的微观形貌与结构、药物释放、力学、抑菌及细胞相容性等性能。结果显示,与水作为固化液相比,随着SFFs溶液(0.017 5~2.1 mg·m L~(-1))的加入,复合材料凝固时间可控,降解率逐渐降低,抗水性增强,韧性提高;同时随丝素纳米纤维含量的增加骨材料抗压强度表现为先增加后减小的趋势,一周内药物释放速率降低;材料同时具有抑菌作用;MTT实验结果显示,加入丝素纳米纤维后与纯的硫酸钙相比MC3T3细胞增殖明显。     

均匀化理论及其在生物力学中的应用

在线弹性理论的范围内,简要介绍了新近发展起来的均匀化理论（ｈｏｍｏｇｅｎｉｚａｔｉｏｎｔｈｅｏｒｙ）,并引入了误差分析方面的一些研究成果．由于均匀化理论可以详尽地考虑材料的微观结构,在生命器官组织的细观力学研究中会起到推动作用．作为应用实例,本文介绍了均匀化理论在密质骨力学性能的数值模拟中的应用．      

8-羟基喹啉快速共沉淀分离富集原子吸收光谱法测定啤酒中的Cu和Pb

研究了用8-羟基喹啉-Mg(Ⅱ)共沉淀体系,以Mn(Ⅱ)为内标,快速共沉淀分离富集啤酒中的铜和铅,并用火焰原子吸收光谱(FAAS)测定的方法。共沉淀受pH值、载体镁和内标锰用量的影响。结果显示在pH为9的条件下,能够定量共沉淀试样中的铜和铅。当试液为100 mL时,方法的检出限分别为铜6.28×10-3 μg·mL-1,Pb 2.26×10-2 μg·mL-1回收率为97.6%～103.0%,基本消除了基体干扰,取得了较为满意的结果。该方法无需收集全部沉淀,与传统的共沉淀方法比较,克服了收集沉淀费时的缺点。方法快速、简便、重现性好。     

A new torsion-rotation fitting program for molecules with a sixfold barrier: Application to the microwave spectrum of toluene

A new program is described for fitting rotation-torsion energy levels in molecules like toluene, in which the frame (C₆H₅) has C_2v symmetry and the methyl top has C_3v symmetry, i.e., for molecules where the internal rotation barrier is expanded in cos6nα, where α is the internal rotation angle and n = 1,2,…. The program is based on the theoretical framework developed by Sørensen and Pedersen in their application of the Longuet-Higgins permutation-inversion group G₁₂ to the microwave spectrum of CH₃NO₂. It is specifically designed for sixfold barrier molecules, and allows the user to select almost any symmetry-allowed torsion-rotation term for inclusion in the fitting Hamiltonian. This program leads to a very successful fit of transitions in the microwave spectrum of toluene characterized by J ? 30, K_a ? 12, and by the free-rotor quantum number ∣m∣ ? 3. In these fits we included both published and rather extensive unpublished new measurements, for which fits using other torsion-rotation programs have not been very successful. The fit presented here uses 28 parameters to give an overall standard deviation of 7.4 kHz for 372 line frequencies, and results in a much improved value for the sixfold barrier for toluene, V₆ = 13.832068(3) cal mol⁻¹.     

A revisit of photoluminescence property for vanadate oxides AVO3 (A:K, Rb and Cs) and M3V2O8 (M:Mg and Zn)

We revisited the vanadium oxide phosphors, AVO₃ (A:K, Rb, and Cs) and M₃V₂O₈ (A:Mg and Zn) for a revaluation of possibility of these compounds for lighting applications, and the internal quantum efficiency (η) and luminescent colour properties for AVO₃ (A:K, Rb, and Cs) and M₃V₂O₈ (A:Mg, and Zn) have been presented. The AVO₃ showed the broadband emission from 380 to 800 nm, and the η for the KVO₃, RbVO₃ and CsVO₃ were 4%, 79% and 87%, respectively. The CIE colour coordinates are located at white region on the chromaticity diagram. The M₃V₂O₈ (A:Mg and Zn) also exhibited a quite broadband emission between 410 and 900 nm, indicating yellow luminescent colour. The Zn₃V₂O₈ showed high η value, 52%, compared to that of the Mg₃V₂O₈ (η=6%). This enhancement of η in the Zn₃V₂O₈ could be due to the increasing exciton diffusion assisted by the hybridizations of Zn 3d and O 2p orbitals for the valence band, and Zn 4s and Ti 3d orbitals for the conduction band.     

Dynamical structure of peptide molecules: Fourier transform microwave spectroscopy and ab initio calculations of N-methylformamide

Rotational spectra of both trans and cis forms of the N-methylformamide normal as well as deuterated (HCONDCH₃, referred to as N-D) species were observed by Fourier transform microwave spectroscopy in the frequency region from 5 to 118 GHz. Samples were prepared in the form of a beam by a pulsed jet valve maintained at 50 °C and were introduced in a high-vacuum cavity cell, with either Ne or Ar as a carrier gas at a backing pressure of 100 kPa. The observed spectra were analyzed to yield molecular parameters including rotational constants and barrier, V₃, to CH₃ internal-rotation: 53.9 (6) and 301 (4) cm⁻¹ for the trans and cis forms of the normal species, respectively, and 41.9 (6) and 309 (4) cm⁻¹ for the trans and cis forms of the N-D species, respectively. Spectra of four trans isotopologues with ¹³C, ¹⁵N, or ¹⁸O singly-substituted in the internal-rotation A state were observed and analyzed to derive the r_s structure of the trans form. For comparison with the experimental data, ab initio calculations were carried out at MP2/6-31G∗∗ level to derive molecular structure, potential barrier to CH₃ internal rotation, and the energy difference between the cis and trans forms. An extensive coupling was found between the CH₃ internal rotation and N-H out-of-plane bending, suggesting that the potential function for the CH₃ internal-rotation deviates considerably from a simple cos(3α) form. The effects of the V₆ term is briefly discussed.     

In-beam spectroscopy of 253, 254No

In-beam conversion electron spectroscopy experiments have been performed on the transfermium nuclei ^{253, 254}No using the conversion electron spectrometer SACRED in nearly collinear geometry in conjunction with the gas-filled separator RITU at the University of Jyv?skyl?. The experimental setup is discussed and the spectra are compared to Monte Carlo simulations. The implications for the ground-state configuration of ²⁵³No are discussed. Received: 21 March 2002 / Accepted: 16 May 2002 / Published online: 31 October 2002 RID="a" ID="a"e-mail: rdh@ns.ph.liv.ac.uk RID="b" ID="b"Present address: GANIL, F-14021 Caen, France. RID="c" ID="c"Permanent address: IReS Strasbourg, IN2P3-CNRS, F-67037-Strasbourg, France. RID="d" ID="d"Present address: CEA/DIF DCRE/SDE/LDN F-91680 Bruyeres-le-Chatel. RID="e" ID="e"Present address: Daresbury Laboratory, Daresbury WA4 4AD, UK. RID="f" ID="f"Permanent address: IPN Lyon, IN2P3-CNRS, F-69037 Lyon, France.