A support vector machine based pharmacodynamic prediction model for searching active fraction and ingredients of herbal medicine: Naodesheng prescription as an example
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Pharmacodynamics
Fraction (chemistry)
This test method covers the procedure for the separation and purification of active ingredient from surfactants and syndet compositions. The separated active ingredient may be used for qualitative examinations. The method also permits the estimation of total active ingredient level present in the sample under test. The method method yields the active ingredient together with other alcohol-soluble materials and therefore is useful only in estimating the actual active ingredient level.
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Relative standard deviation
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Objective To advance prescription quality and standardize prescriptions by analyzing outpatient prescriptions,so as to accommodate the clinic treatment.Methods Judging and analyzing 300 random samples of outpatient prescriptions drew out in the second season in 2010,according to measures for the administration of prescriptions and measures for the administration of prescriptions in hospital.Results There are 144 illogical prescriptions(48.00 percent),114 nonstandard prescriptions(38.00 percent),13 inexact prescriptions(4.33 percent) and 17 excess prescriptions(5.67 percent) in the 300 random samples.Conclusion There is much matter in outpatient prescriptions,and eligible prescriptions are deficient.We shoud study measures for the administration of prescriptions more hard to advance prescription quality and standardize prescriptions,so as to accommodate the clinic treatment.
Outpatient clinic
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Abstract The process of volatilisation of solvents and active ingredients from solid and liquid formulated products has been investigated. Plotting the amount of active ingredient volatilised from a carrier against the square root of time resulted in a linear curve. A simple method of determining the volatility of an active ingredient from layers of its formulated product is also described.
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This test method covers the procedure for the separation and purification of active ingredient from surfactants and syndet compositions. The separated active ingredient may be used for qualitative examinations. The method also permits the estimation of total active ingredient level present in the sample under test. The method method yields the active ingredient together with other alcohol-soluble materials and therefore is useful only in estimating the actual active ingredient level.
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This test method covers the procedure for the separation and purification of active ingredient from surfactants and syndet compositions. The separated active ingredient may be used for qualitative examinations. The method also permits the estimation of total active ingredient level present in the sample under test. The method method yields the active ingredient together with other alcohol-soluble materials and therefore is useful only in estimating the actual active ingredient level.
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API (Active Pharmaceutical Ingredient) means the active ingredient which is contained in medicine. For example, an active ingredient to relieve pain is included in a painkiller. Developing and producing Active Pharmaceutical Ingredients (APIs) includes various processing steps, such as reaction, crystallization, separation and purification, solvent swap, and solvent exchange. Active Pharmaceutical Ingredients or APIs are also known as bulk drugs and a term that is often heard in business news. An active ingredient is the ingredient in a pharmaceutical drug or pesticide that is biologically active. The similar terms active pharmaceutical ingredient and bulk active are also used in medicine, and the term active substance may be used for natural products. Active Pharmaceutical Ingredients are the active ingredients contained in a medicine. The issue of disposal of wastes from these API companies, as well as the development and implementation of efficient collection strategies, is an important concern. This research looks into the factors that have an impact on the disposition of wastes from these companies, and how are these addressed by local government bodies. The pharmaceutical industry discovers, develops, produces, and markets drugs or pharmaceutical drugs for use as medications to be administered to patients with the aim to cure them, vaccinate them, or alleviate symptoms. Pharmaceutical companies may deal in generic or brand medications and medical devices. They are subject to a variety of laws and regulations that govern the patenting, testing, safety, efficacy using drug testing and marketing of drugs.
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Active compound
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This test method covers the procedure for the separation and purification of active ingredient from surfactants and syndet compositions. The separated active ingredient may be used for qualitative examinations. The method also permits the estimation of total active ingredient level present in the sample under test. The method method yields the active ingredient together with other alcohol-soluble materials and therefore is useful only in estimating the actual active ingredient level.
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Nonionic surfactant
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