ABSTRACT
This paper presents an innovated method for the discrimination of groundwater samples in common groups representing the hydrogeological units from where they have been pumped. This method proved very efficient even in areas with complex hydrogeological regimes. The proposed method requires chemical analyses of water samples only for major ions, meaning that it is applicable to most of cases worldwide. Another benefit of the method is that it gives a further insight of the aquifer hydrogeochemistry as it provides the ions that are responsible for the discrimination of the group. The procedure begins with cluster analysis of the dataset in order to classify the samples in the corresponding hydrogeological unit. The feasibility of the method is proven from the fact that the samples of volcanic origin were separated into two different clusters, namely the lava units and the pyroclastic-ignimbritic aquifer. The second step is the discriminant analysis of the data which provides the functions that distinguish the groups from each other and the most significant variables that define the hydrochemical composition of the aquifer. The whole procedure was highly successful as the 94.7 % of the samples were classified to the correct aquifer system. Finally, the resulted functions can be safely used to categorize samples of either unknown or doubtful origin improving thus the quality and the size of existing hydrochemical databases.
Subject(s)
Environmental Monitoring/methods , Geological Phenomena , Groundwater/chemistry , Water Resources , Water , Cluster Analysis , Discriminant Analysis , Environmental Monitoring/statistics & numerical data , Feasibility Studies , Greece , Ions/analysis , Multivariate Analysis , Water/chemistryABSTRACT
Two labdane type diterpenes, labd-13(E)-ene,-8alpha,15-diol (1) and labd-13(E)-ene,-8alpha,15-yl acetate (2) were isolated from the hexane extract of Cistus creticus subsp. eriocephalus (Viv.) Greuter & Burdet leaves, while (+)-19-acetoxy-cis-clerodan-3-en-15-oic acid (3) was isolated from the hexane extract of Cistus monspeliensis L. leaves. The compounds were examined for their in vitro cytostatic and cytotoxic activity against nine human leukemic cell lines, three of which exhibited a multidrug resistant phenotype. They were also evaluated for their anti-inflammatory activity in vivo on the back of hairless mice. The cytostatic and cytotoxic activity of the tested diterpenes followed the order 1>2>3. Topical application of the diterpenes on barrier disrupted skin did not seem to have a significant contribution to the repair rate of the skin barrier.
Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Antineoplastic Agents, Phytogenic/pharmacology , Cistaceae/chemistry , Diterpenes/pharmacology , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Antineoplastic Agents, Phytogenic/chemistry , Cell Line , Diterpenes/chemistry , Diterpenes/isolation & purification , Humans , Mice , Plant Extracts/pharmacology , Plant Shoots/chemistry , Skin , Tumor Cells, CulturedABSTRACT
Essential oils and hexane extracts from Cistus monspeliensis L. leaves and fruits were analysed by GC-MS. Manoyl oxide and its isomers, 3 beta-hydroxy-manoyl oxide, 3 beta-hydroxy-13-epi-manoyl oxide, as well as 3 beta-acetoxy-13-epi-manoyl oxide were detected for the first time in C. monspeliensis L. Ent-13-epimanoyl oxide was isolated from the hexane extract of leaves and its structure was determined using spectroscopic methods. In vitro cytotoxic activity of ent-13-epi-manoyl oxide and mixtures of manoyl oxide isomers at 10(-4) M concentrations ranged from 11.1 to 32.2% of the activity for a vinblastine control evaluated against nine leukemic cell lines. The results showed that the manoyl oxide isomer mixtures as well as ent-13-epi-manoyl oxide exhibited a slight growth inhibiting activity.
Subject(s)
Oils, Volatile/isolation & purification , Plant Extracts/isolation & purification , Plants, Medicinal/chemistry , Terpenes/isolation & purification , Leukemia/drug therapy , Molecular Structure , Oils, Volatile/pharmacology , Plant Extracts/pharmacology , Plant Leaves/chemistry , Structure-Activity Relationship , Terpenes/pharmacology , Tumor Cells, Cultured/drug effects , Vinblastine/therapeutic useABSTRACT
The composition of the essential oils of nine populations of Cistus parviflorus L., from Crete (Greece) and their interpopulation variability, were investigated by GC-MS. 114 compounds were identified representing an average of 85-96% of oil composition. Labdane diterpenes were detected and identified in the essential oils of Cistus parviflorus L. for the first time. The results obtained from GC-MS analysis of the volatile oils were submitted to principal component and chemometric cluster analysis. Two main chemotypes (clusters) were differentiated; the first of West Crete and the second of East Crete. Carvacrol, caryophyllene oxide, alpha-epi-cadinol, abietatriene, 4-epi-dehydroabietol, dehydro abietol, cis-ferruginol and manoyl oxide mixture of isomers are the main constituents, while oxygenated sesquiterpenes as well as diterpenes have been found in high percentage composition.
ABSTRACT
Two myricetin derivatives, the 3,7, 4('), 5(')- tetramethyl ether of myricetin (1), isolated from the hexane extract of Cistus monspeliensis, and its 3('),5-diacetyl derivative (2) which was synthesized, and the parent compound, myricetin (3), were examined for their in vitro cytotoxic activity against nine human leukemic cell lines, two of which were mdr cell lines. Compound 2 exhibited higher cytostatic and cytotoxic activities in comparison to compound 1, while compound 3 was inactive against all tested cell lines. Vinblastine was used as a control.
