Carboplatin

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Structural formula
Structure of carboplatin
General
Non-proprietary name Carboplatin
other names

Diammine platinum (II) cyclobutane 1,1-dicarboxylate

Molecular formula C 6 H 12 N 2 O 4 Pt
External identifiers / databases
CAS number 41575-94-4
EC number 255-446-0
ECHA InfoCard 100.050.388
PubChem 10339178
DrugBank DB00958
Wikidata Q415588
Drug information
ATC code

L01 XA02

Drug class

Cytostatics

properties
Molar mass 371.25 g mol −1
safety instructions
Please note the exemption from the labeling requirement for drugs, medical devices, cosmetics, food and animal feed
GHS labeling of hazardous substances
07 - Warning 08 - Dangerous to health

danger

H and P phrases H: 302-312-317-332-334-360
P: 201-261-280-308 + 313
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Carboplatin is a very common cytostatic drug (used to fight cancer ). The chemical structure contains a complex bonded platinum atom , it is a cisplatin derivative. The effect against cancer cells is based on a cross-linking of the DNA molecules (genetic material), which thereby become inoperable. The cell metabolism is hindered and the cell dies. Like other cytostatic agents, carboplatin acts in this way not only on rapidly growing tumor cells , but to a certain extent also on healthy body cells. It is given intravenously.

Mechanism of resistance

Note the cross-resistance with cisplatin .

indication

Application areas for carboplatin are bronchial carcinoma , ovarian carcinoma , breast carcinoma and testicular cancer . Carboplatin is administered as an infusion within 15 to 60 minutes, usually at intervals of 4 weeks, and is used almost exclusively in combination with other chemotherapeutic agents (combination chemotherapy ). A combination of newer cytostatic agents such as gemcitabine , vinorelbine or taxanes with the platinum salts cisplatin or carboplatin has established itself as the standard therapy worldwide.

unwanted effects

Vomiting (therefore often simultaneous administration of antiemetics ), hearing damage or ringing in the ears ( tinnitus ), dizziness , allergies , nerve damage, abdominal pain , constipation, diarrhea , damage to blood-forming cells of the bone marrow . In addition, carboplatin is nephrotoxic (it damages the kidneys ).

Trade names

Monopreparations

Axicarb (D), Carbo-cell (D), Carbomedac (D), Haemato-carb (D), Neocarbo (D), Paraplatin (CH), Ribocarbo (D), various generics (D, A, CH)

Web links

Individual evidence

  1. a b Carboplatin data sheet from Sigma-Aldrich , accessed on March 15, 2011 ( PDF ).Template: Sigma-Aldrich / name not given
  2. Single-dose carboplatin is just as effective in testicular cancer as radiotherapy .
  3. Cisplatin versus carboplatin in NSCLC in advanced stages ( Memento from September 29, 2007 in the Internet Archive ) (PDF; 56 kB).
  4. Red List online, as of September 2009.
  5. AM comp. d. Switzerland, as of September 2009.
  6. AGES-PharmMed, as of September 2009.