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1996 Vol. 14, No. 2

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OTC system and discussion about its out-carrying in our country
Wang Shimin, Zhang Jun, Wang Xiaoli
1996, (2): 67-72.
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This article systematically introduces the conception of OTC, the evolution of American OTC system and the external classification of drugs. Nowaday condition, future derection and market tendency of OTC are revealed, the reason why OTC system is so popular is analized, some questions related to creating characteristic OTC system in China are discussed.
1996, (2): 73-74.
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1996, (2): 74-77.
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1996, (2): 77-80.
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1996, (2): 81-82.
Abstract(3327) PDF (1770KB)(1886)
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Preparation and clinical effect study of laofu shuan
Du Qingyun, Hu Yongshi, Zhang Mingqiong, Liu Biaosheng
1996, (2): 82-84.
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The prescription and preparing method of Laofu Shuan was presented in this paper. 107 climacteric female cases with obvious vaginitis syptoms and physical signs were chosen and studied of PH, smear examination and bacterial culture of vagina secretion before and after treatment.The results showed that the cure rate was 82.49%, the improving rate was 17.5% and the total effective rate was 100%. 79 cases were reexaminated in 1.5yr and indicated the cure rate was 69.9% and the effective rate 25.3%, The recurrence was 5.06% and the total effective rate was 94. 94%.
1996, (2): 85-86.
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1996, (2): 86-88.
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1996, (2): 88-90.
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1996, (2): 90-90.
Abstract(1952) PDF (709KB)(372)
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1996, (2): 91-95.
Abstract(2629) PDF (2457KB)(2465)
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1996, (2): 95-96,72.
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1996, (2): 97-100.
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1996, (2): 100-101.
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1996, (2): 102-103.
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Progress in sustained-release microgranules
Jin Honghua, Zhang Hengbi
1996, (2): 103-107.
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The paper reported the produce、development、manufacturing process and dissolving mechanism of sustained-release microgranules. The paper also reported new technology in manufacturing sustained-release microgranules and new industrial art and new Pharmaceutical aids.
1996, (2): 107-109,119.
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1996, (2): 110-111.
Abstract(1859) PDF (1997KB)(1069)
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1996, (2): 111-113.
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Practice of study on pharmaceutical analysis methodlgy and quality assurance system
Tao Qiaofeng
1996, (2): 113-116.
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This paper discussed the procedures for validating pharmaceutical analysis methods and selecting the validation parameters.The importance was stressed for developing the quality assurance system.
UV spectrophotometric determination of Naproxen tablet
Huang Jingqiang, Fu lidao
1996, (2): 116-118.
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A UV spectrophotometric method for the determination of Naproxen tablet was studied. The results showed that the method was simple,rapid and accurate and was not interfered by vehicle, The absorption coefficient (E1cm1%) of Naproxen in alcohlol was 85.6 and RSD was 0.90%(n=20).The average recovery was 100.4% and RSD was 0.51% (n=51). No significant difference was noticed between the results of this method and the volumetric method.
Quantitative determination of methocarbamol Capsules by UV Spectrophotometry
Li Jiafu, Wang Guohua
1996, (2): 118-119.
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A UV-Spectrophotometric method for the quantitative determination of methocarbamol capsules was described. The absorbances were measured at 274nm. The average recovery was 99.5% (RSD=0.25%,n=5). The results showed that the method was simpler, satisfactory and suited to rapid analysis for the medium and product.
1996, (2): 120-121.
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A survey of prescriptions of antipyretic analgesic, NSAIDs consumption
Chen Miaoying
1996, (2): 121-124.
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This paper analyzed 12518 OPD prescription of Huashan Hospital during January, 1994 to December, 1994. The results showed that antipyretic analgesic, NSAIDs precriptions accounted for 12.1% of the total precriptions, of which, 93.92% precriptions can be seen using these drugs alone, and DUI of the most drugs less than 1, so drugs abuse in dosage were insignificant。
1996, (2): 124-128.
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1996, (2): 128-128.
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