医药类专业物理课程教学存在的问题及对策

根据对国内69所普通高等院校医药类专业（本科）物理课程教学现状调查的结果,分析了在我国高等教育进入“大众化教育”的形势下,医药类专业物理课程教学中存在的4个急需解决的问题,指出了医药类专业物理课程教学改革的方向,并介绍了我们所做的一些工作。     

Investigation of capillary electrophoresis-laser induced fluorescence as a tool in the characterization of sewage effluent for fluorescent acids: determination of salicylic acid

The investigation of emerging contaminant issues is a proactive effort in environmental analysis. As a part of this effort, sewage effluent is of current analytical interest because of the presence of pharmaceuticals and their metabolites and personal care products. The environmental impact of these components is still under investigation but their constant perfusion into receiving waters and their potential effect on biota is of concern. This paper examines a tool for the characterization of sewage effluent using capillary electrophoresis-laser induced fluorescence (CE-LIF) with a frequency-doubled laser operated in the ultraviolet (UV). Fluorescent acidic analytes are targeted because they present special problems for techniques such as gas chromatography-mass spectrometry (GC-MS) but are readily accessible to CE-LIF. As an example of the application of this tool, salicylic acid is determined near the 100 ng/L (7 x 10(-10) M) level in sewage effluent. Salicylic acid is a metabolite of various analgesics. Relatively stable in the environment, it is a common contaminant of municipal sewage systems. Salicylic acid was recovered from freshly collected samples of the effluent by liquid-liquid extraction. Confirmation of identity was by electron ionization GC-MS after conversion of the salicylic acid to the methyl ester by means of trimethylsilyldiazomethane. CE-LIF in the UV has revealed more than 50 individual peaks in the extract and a background response that suggests a large and indeterminate number of additional compounds are present. These data together with complementary techniques provide information on the complexity and components in these effluent streams.     

The accuracy of signal intensity measurements in magnetic resonance imaging as evaluated within the knee.

Quantitative signal intensity measurements are being utilized in both clinical and research magnetic resonance imaging protocols. This paper addresses three questions in quantitative MRI measurements as evaluated within the knee: 1) the accuracy of quantitative measurements; 2) improvement of accuracy by phantom normalization; and 3) the amount of signal change that is clinically significant. Seven normal subjects were imaged on three different days within a 1-wk period. Test-tube phantoms of manganous chloride (MnCl2) were imaged posterior to the knee and were used to normalize each image. The variation in signal intensity within the same subject averaged 20% for both the anterior cruciate ligament (ACL) and the posterior cruciate ligament (PCL). The phantom variation was approximately 18%. Signal intensity normalization by background subtraction, background division, phantom division, or a combination of subtraction and division did not significantly improve either the phantom variation or the ligament variation. Given that an individual ligament intensity will be measured with standard errors of +/- 20% of its value, we calculated the minimum increase in signal intensity to be considered abnormal relative to a normal ligament. A relative signal increase of 46% can be considered pathologic with 95% confidence. These findings emphasize that quantitative measurements must be carefully assessed when being applied in clinical settings.     

Measurement of the negative muon anomalous magnetic moment to 0.7 ppm

The anomalous magnetic moment of the negative muon has been measured to a precision of 0.7 ppm (ppm) at the Brookhaven Alternating Gradient Synchrotron. This result is based on data collected in 2001, and is over an order of magnitude more precise than the previous measurement for the negative muon. The result a(mu(-))=11 659 214(8)(3) x 10(-10) (0.7 ppm), where the first uncertainty is statistical and the second is systematic, is consistent with previous measurements of the anomaly for the positive and the negative muon. The average of the measurements of the muon anomaly is a(mu)(exp)=11 659 208(6) x 10(-10) (0.5 ppm).     

Quasi-Differential Posets and Cover Functions of Distributive Lattices II: A Problem in Stanley’s <Emphasis Type="Italic">Enumerative Combinatorics</Emphasis>

A distributive lattice L with 0 is finitary if every interval is finite. A function f:₀₀ is a cover function for L if every element with n lower covers has f(n) upper covers. All non-decreasing cover functions have been characterized by the author ([2]), settling a 1975 conjecture of Richard P. Stanley. In this paper, all finitary distributive lattices with cover functions are characterized. A problem in Stanleys Enumerative Combinatorics is thus solved. 2000 Mathematics Subject Classification. 06A07, 06B05, 06D99, 11B39     

The complete 1H and 13C chemical shift assignments of a cyclopropylpyrroloindole analog: Adozelesin

The ¹H and ¹³C nmr spectral assignments of [7bR]-N-[2-[(4,5,8,8a-tetrahydro-7-methyl-4-oxocyclo-propa[c]pyrrolo[3,2-e]indol-2(1H)-ylcarbonyl]-1H-indol-5-yl]-2-benzofurancarboxamide (Adozelesin) (1) are described. Complete and unambiguous assignments of the hydrogen and carbon spectra were made using a combination of conventional homonuclear and gradient-selected inverse-detected heteronuclear nmr experiments: double quantum filtered ¹H-¹H correlation spectroscopy (COSY), gradient-selected heteronuclear single quantum coherence spectroscopy (gs-HSQC), and gradient-selected heteronuclear multiple bond coherence spectroscopy (gs-HMBC). The enhanced sensitivity of these experiments allowed a smaller sample concentration and shorter spectral collection times for a full nmr analysis of this compound. The nmr data corroborates the published structure of this compound.     

The elastic behaviour of InBi single crystals

Ultrasonic wave velocities have been measured by the pulse echo technique at 15MHz in single crystals of InBi grown by zone-melting. The elastic stiffness constant set has been computed from the velocity data by a least-mean-squares procedure. The elastic behaviour of this metallic compound is quite different in kind from that of the semiconducting III-V crystals; the volume compressibility does not follow Keyes' generalisation for the other III-V compounds. The elastic properties of InBi have been found to show the characteristics of a layer-like crystal with weak interlayer binding; this finding is illustrated by the linear compressibilities and by a compilation of cross-sections of the wave velocity and Young's modulus surfaces. The Debye temperature is 115°K.     

Fixed charge problems with identical fixed charges

The general problem considered by this paper is a special case of the fixed-charge problem. The further condition imposed is that all variables have the same associated fixed-charge. The problem is discussed in the context of a known commercial application, that being the cutting stock problem. The situation considered is that of cutting given numbers of small rectangles from large rectangular stock-plates. In many such situations major aims are to have low stock-plate usage and a low number of setups of the cutting equipment. These represent conflicting objectives capable of being combined by the use of fixed charges upon the setups but this paper presents an alternative approach incorporating direct manipulation of the number of setups involved in the solution. This approach is compared to a solution technique for the general fixed-charge problem.     

An asymmetric synthesis of (2S,5S)-5-substituted azepane-2-carboxylate derivatives

To facilitate a drug discovery project, we needed to develop a robust asymmetric synthesis of (2S,5S)-5-substituted-azepane-2-carboxylate derivatives. Two key requirements for the synthesis were flexibility for elaboration at C5 and suitability for large scale preparation. To this end we have successfully developed a scalable asymmetric synthesis of these derivatives that starts with known hydroxy-ketone 8. The key step features an oxidative cleavage of aza-bicyclo[3.2.2]nonene 14, which simultaneously generates the C2 and C5 substituents in a stereoselective manner.