adulterations of herbal drugs


  Control Measures for Deterioration



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Adultration

3.3.9  Control Measures for Deterioration

The container utilized for storage and its enclosure must not communicate physically or synthetically with the material 

inside in any way that would adjust its arrangement. A firmly closed compartment must shield the substance from extrane-

ous issues or from loss of the material while handling and a firmly shut holder must shield the material from blooming

deliquescence, or dissipation under handling at typical capacities. The holding area ought to be kept clean and spillage 

must not be permitted to enter breaks or through holes. Occasionally showering the premises with insecticides will halt the 

spread of infestation. The standards that apply to the control of invasion in warehouses are also appropriate to small-scale 

stockpiling. Good housekeeping is the most extreme basic. Each stock ought to be assessed routinely and tainted material is 

best destroyed by burning. In this regard, a quick swing over to wipe out the impacts of disintegration because of both the 

essential and auxiliary factors, as noted above, is desirable. Cool, dry conditions are the most reasonable to hinder living 

organisms. As every single living organism requires water, extremely dry medications ought to be resistant to auxiliary de-

cay. In some cases, herbal therapeutic items obtained by the herbalist may now have been cleaned, which is usually accom-

plished by treatment of the mass transfer with ethylene oxide or methyl bromide under controlled conditions. Medications 

so treated should be subject to a satisfactory limit for harmful buildups, for example, for Senna cases 50 ppm of ethylene 

oxide is the limit. Various assessment procedures for herbal products, from the point of view of cost control and for deciding 

substituents, will be specified in later sections.




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