Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
Add more filters










Publication year range
1.
J Pharm Biomed Anal ; 157: 84-91, 2018 Aug 05.
Article in English | MEDLINE | ID: mdl-29775811

ABSTRACT

In this study, a LC-MS/MS method for the measurement of docetaxel in Dried Blood Spots (DBS) samples was developed and validated. Docetaxel was extracted from 8 mm DBS punch with a mixture of methanol and acetonitrile (9:1, v/v). The chromatographic separation occurred in an Acquity® C18 column (150 × 2.1 mm, 1.7 µm) eluted with a mixture of water and acetonitrile plus 0.1% formic acid (45:55, v/v). Total analytical run time was 7 min. The method was linear from 50 to 3000 ng ml-1. Precision assays showed CV% < 9.8% and accuracy between 99 and 103%, mean recovery was 81%. The method was applied in the determination of the docetaxel in 31 patients, after collection of two paired venous blood and DBS samples, following a limited sampling strategy protocol. The analyte was stable in DBS for 18 days at 25 °C and 9 days at 45 °C. The interval of docetaxel concentrations measured in DBS collected before the end of the infusion was 756-3047 ng ml-1 and 60 ±â€¯10 min after the end of the infusion was 57-331 ng ml-1. AUC values calculated from DBS-derived estimated plasma concentrations (EPC) represented on average 100% of those obtained in plasma samples of 3.1 mgh/l (2.4-4.9 mg h/l). There was a 93% agreement between the classification of patients as within or without the therapeutic range by plasma and EPC AUC. These findings support the clinical use of DBS sampling for routine therapeutic drug monitoring of docetaxel.


Subject(s)
Chromatography, Liquid/methods , Dried Blood Spot Testing/methods , Tandem Mass Spectrometry/methods , Taxoids/blood , Docetaxel , Drug Monitoring/methods , Humans , Reproducibility of Results
2.
Science ; 293(5530): 629-37, 2001 Jul 27.
Article in English | MEDLINE | ID: mdl-11474098

ABSTRACT

Ecological extinction caused by overfishing precedes all other pervasive human disturbance to coastal ecosystems, including pollution, degradation of water quality, and anthropogenic climate change. Historical abundances of large consumer species were fantastically large in comparison with recent observations. Paleoecological, archaeological, and historical data show that time lags of decades to centuries occurred between the onset of overfishing and consequent changes in ecological communities, because unfished species of similar trophic level assumed the ecological roles of overfished species until they too were overfished or died of epidemic diseases related to overcrowding. Retrospective data not only help to clarify underlying causes and rates of ecological change, but they also demonstrate achievable goals for restoration and management of coastal ecosystems that could not even be contemplated based on the limited perspective of recent observations alone.


Subject(s)
Ecosystem , Fishes , Marine Biology , Animals , Archaeology , Bacteria , Cnidaria , Conservation of Natural Resources , Eutrophication , Geologic Sediments , Humans , Seaweed , Shellfish , Time Factors
3.
Trends Ecol Evol ; 14(7): 261-2, 1999 Jul.
Article in English | MEDLINE | ID: mdl-20109434
4.
Trends Ecol Evol ; 11(7): 278-80, 1996 Jul.
Article in English | MEDLINE | ID: mdl-21237842
5.
Science ; 224(4646): 283-5, 1984 Apr 20.
Article in English | MEDLINE | ID: mdl-17734914

ABSTRACT

Strong winter storms in southern California destroyed most of the canopy ofthe giant kelp Macrocystis pyrifera but not the patches of understory kelps in the Point Loma kelp forest near San Diego. Subsequent massive recruitment of Macrocystis juveniles and adults that survived the storms had low survival in the summer during the California El Niño of 1983. The combined disturbance may have long-lasting structural consequences for this community because, once established, the understory patches can resist invasion by Macrocystis.

6.
Science ; 196(4287): 324-6, 1977 Apr 15.
Article in English | MEDLINE | ID: mdl-847476

ABSTRACT

Coexisting sea urchins Strongylocentrotus purpuratus and S. franciscanus exhibit different recruitment patterns. Juveniles of the former species are found in a variety of habitats, whereas juveniles of the latter occur almost exclusively under the spine canopy of conspecific adults. The commercial harvest of S. franciscanus thus seems to affect nursery grounds as well as the reproductive potential of exploited populations.


Subject(s)
Sea Urchins/physiology , Animals , Diet , Ecology , Fisheries , Reproduction , Sea Urchins/growth & development , Species Specificity
7.
J Exp Zool ; 197(1): 31-57, 1976 Jul.
Article in English | MEDLINE | ID: mdl-939961

ABSTRACT

The surface coats of sea urchin eggs and the events of fertilization which take place on these surfaces were examined with the scanning electron microscope (SEM). Gametes of Stronglyocentrotus purpuratus and Lytechinus pictus were considered in detail; eggs of seven other echinoids were examined for comparative purposes. Jelly coats, preserved by varying the pH of fixation, were found to vary in morphology and solubility properties between species. The vitelline layers of the nine echinoids are characterized by arrays of projections which are impressions of cytoplasmic microvilli in the vitelline layer. After sperm bind to the egg surface via the acrosomal process, fine filaments, apparently an egg response to insemination, further connect some sperm heads and tails to the egg. The cortical reactions spread out as a wave from where the fertilizing sperm fused with the egg; separation of the vitelline layer proceeds as a smooth wave from S. purpuratus eggs and as a series of localized separations in L. pictus eggs. The fertilization membranes of S. purpuratus and Allocentrotus fragilis zygotes are expanded replicas of their respective vitelline layers, suggesting that fertilization membranes are formed by an unfolding of the vitelline layer.


Subject(s)
Fertilization , Ovum/ultrastructure , Vitelline Membrane/ultrastructure , Animals , Cytoplasmic Granules/ultrastructure , Female , In Vitro Techniques , Male , Sea Urchins , Spermatozoa/ultrastructure
9.
Science ; 179(4074): 685-8, 1973 Feb 16.
Article in English | MEDLINE | ID: mdl-4734353

ABSTRACT

Scanning electron microscopy of the outer surface of sea urchin eggs sampled at intervals during the first 3 minutes after insemination reveals the detailed structural changes of the vitelline layer during its transformation into the fertilization membrane. A sperm attachment-detachment sequence is described for the large number of sperm which transitorily bind every egg during fertilization.


Subject(s)
Fertilization , Microscopy, Electron, Scanning , Ovum/cytology , Sea Urchins/cytology , Spermatozoa/cytology , Animals , Female , Male , Time Factors , Vitelline Membrane
SELECTION OF CITATIONS
SEARCH DETAIL