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Random collections of plants have been screened by the National Cancer Institute's screening program for almost two decades. The WARF Institute, Inc. (Madison, Wis) has been preparing most of the crude plant extracts for antitumor screening for the past 14 years. This paper describes our present method of extraction for preparation of crude plant extracts for screening and presents a history of past procedures used for the extraction of plant materials. Wherever possible, screening statistics have been included for plants which have been extracted by the various procedures.
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The authors developed a thin-layer chromatographic technique for the separation of carbamate pesticides from plant material and an enzymatic method for their determination. The cellulose plates were impregnated with polar substances (ethylene glycol, triethylene glycol and beta,beta'-oxydipropionitrile). n-Heptane/chloroform and iso-octane/dioxane served as solvents. The slight enzyme-inhibiting effect and the colouration of the plant extracts render the detection of the pesticides difficult. Nevertheless, the separation and the enzymatic detection of Methomyl, Carbaryl, Baygon and Aldicarb could be achieved. The Rf values of the carbamates are not influenced by the kind (apples, pears, onions) and the quantity (50--200 mg) of the plant material.
Crude plant products were first tested in the Drug Research and Development Program, Division of Cancer Treatment, NCI, in 1956. The first materials were voluntarily submitted and later materials were acquired through various contracts. A review is given of the tumor systems which have been used for the evaluation of these plant products and of in vitro assays utilized to expedite fractionation and isolation.
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The aqueous extracts from 178 kinds of medicinal plants belonging to 69 families were examined from the point of their virustatic activity against herpes-, influenza-, vaccine- and poliovirus. 75 kinds proved to be virustatic against one or more kinds of virus. Nearly one-third of the active plants belong to families that are known as especially rich in tannin. Besides the virustatic activity a great number of extracts showed also a cytostatic activity.
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The cytostatic activity of aqueous, alcoholic and ketonic extracts of 9 species of superior plants of the families Fitolacaceae, Compositae, Moraceae, Zingiberaceae, Martiniaceae, Mirtaceae, Verbenaceae and Annonaceae was assessed. The Kubas microbiologic method and the fungus Ascomiceto Neurospora crassa were used in the assessment. The fungus growth was measured in millimeters. Inhibition percentages for every case regarding control are reported. The best results were obtained from Annona muricata, Costus spiralis, Cecropia peltata, Xanthium chinense and Pluchea adorata extracts.
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The study of the cytostatic activity of aqueous, alcoholic and ketonic extracts from 18 parts of 9 species of superior plants of the families Araceae, Borraginacease, Burseraceae, Cesalpinaceae, Meliaceae, Compositae, Rebiaceae, Cruciferaceae and Verbenaceae using the microbiologic method of described by Kubas in 1972 is pursued. The best results were obtained from Hamelia patens. Lippia alba, Lepidium virginicum, Cassia ligustrina, Bursera simaruba and Heliotropium campechianum extracts.
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Antiserum specificity for digoxin was demonstrated by means of three tests: cross-reactivities test, dilutions test and thin-layer chromatography test. The cross-reactivities test examined quantitatively the cross-reactivities with specific compounds and provided an explanation for the basis of the dilutions test. The dilutions test was used to demonstrate the suitability or unsuitability of the antiserum for use in the radioimmunoassay of digoxin in a crude biological sample. The tlc test examined for antiserum cross-reactivity with digoxin and related compounds in a crude extract.
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