ArtNr |
S1215-10mM |
Hersteller |
Selleckchem
|
CAS-Nr. |
41575-94-4 |
Menge |
10 mM/1 ml |
Kategorie |
|
Typ |
Inhibitors |
Specific against |
other |
ECLASS 10.1 |
32160490 |
ECLASS 11.0 |
32160490 |
UNSPSC |
12000000 |
Alias |
JM-8, CBDCA, DNA/RNA Synthesis |
Similar products |
Carboplatin(JM-8 |
Lieferbar |
|
Administration |
Administered via i.p. |
Animal Models |
The A2780 human ovarian cancer cell line is grown as a subcutaneous xenograft in female athymic NCr nude mice (nu/nu) in each flank. |
Cell lines |
A2780, SKOV3, IGROV-1 and HX62 |
Clinical Trials |
Carboplatin is currently in Phase II clinical trials in patients with Recurrent, Ovary, Fallopian Tube, and Primary Peritoneal Cancer. |
Concentrations |
0-200 uM |
Description |
Carboplatin is a DNA synthesis inhibitor by binding to DNA and interfering with the cell's repair mechanism. |
Dosages |
<=60 mg/kg |
Features |
Carboplatin is a DNA synthesis inhibitor. |
Formulation |
Carboplatin is dissolved in 43% ethanol, 33% polypropylene glycol and 24% cremaphor diluted 1:7 with sterile water. |
In vitro |
Carboplatin exhibits an inhibitory effect on cell proliferation in a human ovarian cancer cell line panel, including A2780, SKOV3, and IGROV-1 cells with IC50 of 6.1 uM, 12.4 uM and 2.2 uM, respectively. [1] Carboplatin also show the anti-proliferative activities in lung carcinoid cell line, such as UMC-11, H727, and H835 cells with IC50 of 36.4 uM, 3.4 uM and 35.8 uM, respectively. [2] |
In vivo |
In A2780 tumor xenografts, Carboplatin (60 mg/kg via i.p.) given as single agents shows a modest antitumor effect with the relative tumor volumes on day 6 of 8.4 compared to the control of 11.9, and the day 6 tumor weights relative to control (T/C) of 67%. [1] For the VC8 (Brca2-deficient) xenografts, Carboplatin treatment delays tumor growth and reduces tumor mass by 42% compared to the vehicle group. [3] |
Incubation Time |
72 hours |
Method |
3-(4, 5-dimethylthiazol-2yl)-2, 5-diphenyltetrazolium bromide (MTT) assays: Exponentially growing A2780, SKOV3, IGROV-1 and HX62 ovarian cancer cells are plated in 96 well plates. A range of drug concentrations are added and the plates are incubated for 72 hours to allow for 34 doubling times. Each experiment is carried out in triplicate. Sulforhodamine B (SRB) assays: Exponentially growing A2780 cells are plated in 96 well microtitre plates. For experiments studying concomitant exposure, cells are exposed to increasing concentrations of both drugs for 96 hours. For experiments studying the effect of sequence of exposure to 17-AAG or carboplatin cells are exposed to increasing concentrations of 17-AAG or carboplatin for 24 hours. A period of 24-hour exposure to the first agent is chosen so that the A2780 cells would be exposed to the first drug for at least one doubling time (18-24 hours). The cells are then washed with sterile phosphate buffered saline and the medium is replenished. Following this, the second drug (to which the cells are not exposed to in the first 24 hours) or medium is added for 96 hours. All experiments are carried out in triplicate. The results of combination studies are analyzed using the well-established principles of median effect analysis method. The effects of the combination are calculated using an in-house spreadsheet. |
Molecular Weight (MW) |
371, 25 |
Picture ChemicalStructure Description |
Carboplatin Chemical Structure |
Picture Description 1 |
Data independently produced by, , , Dr. Helen Sadik, of Johns Hopkins University, Carboplatinpurchased from Selleck, A. MCF10A-Ras overexpressing a vector control or the gene of interest (GeneX), or MCF7 expressing a scramble or a siRNA for the geneX were treated with DMSO or with Carboplatin for 24h. Resistant colonies were allowed to grow for 2 weeks, and are then stained with Crystal Violet. B. Quantification of the results. |
Picture Description 2 |
Data independently produced by, , , Dr. Helen Sadik, of Johns Hopkins University, Carboplatinpurchased from Selleck, Cells were seeded in 96 well paltes, and then treated with the indicated concentration of Carboplatin for 48h. Cell survival was measured by a standarad MTT assay. |
Solubility (25C) |
DMSO <1 mg/mL, Water <1 mg/mL, Ethanol <1 mg/mL |
Storage |
2 years -20CPowder, 2 weeks4Cin DMSO, 2 months-80Cin DMSO |
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