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CONTENT
• History
• Platinum complexes
• Cancer therapy
• Advantages
• Disadvantages
• Future updates
• Market availability
• Conclusions
• References
HISTORY
(cis platin)
• 1844 it was first created by Italian chemist Michele
Peyrone
• Barnett Rosenberg 1965
(carboplatin)
• 1971 by Bristol-Myers Squibb
(Oxaliplatin)
• 1976 World Health Organization's List of Essential
Medicines
PLATINUM COMPLEXES
 Cis-platinum
 Carbo-platinum
 Oxaliplatin
oxaliplatin
corboplatin
Cancer therapy
Advantages
 Charge variations
 Structure and bonding
 Matel ligind interaction
 Lewis acid properties
 Partially field d-orbital
 Redox activity
 Maximum survival rate
 Apoptosis
 Selective targets
Disadvantages
 Kidney damage
 Anemia
 Cough
 Platelet disorders
 Drug resistance
 Neurotoxicity
 Alimentary canal toxicity
 Hair lose
Future updates
 Dicycloplatin is a reformulation of the drug
carboplatin by Sopo-Xingda Pharmaceutical and
Bioplatin AG and is currently under clinical trial
evaluation in China.
Market availability
Platinum based Cancer Drug Market Segment by Type
covers:
 Cisplatin (Platino)
 Oxaliplatin (Paraplatin)
 Carboplatin (Eloxatin)
 Other
Conclusion
 Anti-cancer drug cisplatin and could be able to target cancer cells
without producing the ototoxic side-effects commonly
associated with this chemotherapy compound.
 Addition of steric bulk cis to the coordinating center of a
monofunctional DNA compound is one strategy that has
emerged in the development of new chemotherapy drug
candidates.
 Our results suggest that triamine-ligated complexes with this
form of steric bulk can exhibit nuclear compartmental targeting
and anti-cancer cell effects competitive with their heterocyclic
ligated counterparts.
 Further, although the triamine- and heterocyclic ligated
complexes produce auditory threshold shifts similar to cisplatin,
unlike cisplatin, the monofunctional compounds produce
virtually no effect on auditory hair cell density.
References
 1.Langer T, am Zehnhoff-Dinnesen A, Radtke S, Meitert J,
Zolk O. Understanding platinum-induced ototoxicity.
Trends Pharmacol Sci. 2013;34: 458–69. pmid:23769626
 2.Karasawa T, Steyger PS. An integrated view of cisplatin-
induced nephrotoxicity and ototoxicity. Toxicol Lett.
2015;237: 219–27. pmid:26101797
 And Cancer Therapy. Cancer. 2016;122: 1647–58.
pmid:26859792
 4.Lanvers-Kaminsky C, Zehnhoff-Dinnesen AA, Parfitt R,
Ciarimboli G. Drug-induced ototoxicity: Mechanisms,
Pharmacogenetics, and protective strategies. Clin
Pharmacol Ther. 2017;101: 491–500. pmid:28002638

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Medicinal application of organometallic compounds

  • 1.
  • 2. CONTENT • History • Platinum complexes • Cancer therapy • Advantages • Disadvantages • Future updates • Market availability • Conclusions • References
  • 3. HISTORY (cis platin) • 1844 it was first created by Italian chemist Michele Peyrone • Barnett Rosenberg 1965 (carboplatin) • 1971 by Bristol-Myers Squibb (Oxaliplatin) • 1976 World Health Organization's List of Essential Medicines
  • 4. PLATINUM COMPLEXES  Cis-platinum  Carbo-platinum  Oxaliplatin oxaliplatin corboplatin
  • 6.
  • 7.
  • 8. Advantages  Charge variations  Structure and bonding  Matel ligind interaction  Lewis acid properties  Partially field d-orbital  Redox activity  Maximum survival rate  Apoptosis  Selective targets
  • 9. Disadvantages  Kidney damage  Anemia  Cough  Platelet disorders  Drug resistance  Neurotoxicity  Alimentary canal toxicity  Hair lose
  • 10. Future updates  Dicycloplatin is a reformulation of the drug carboplatin by Sopo-Xingda Pharmaceutical and Bioplatin AG and is currently under clinical trial evaluation in China.
  • 11. Market availability Platinum based Cancer Drug Market Segment by Type covers:  Cisplatin (Platino)  Oxaliplatin (Paraplatin)  Carboplatin (Eloxatin)  Other
  • 12. Conclusion  Anti-cancer drug cisplatin and could be able to target cancer cells without producing the ototoxic side-effects commonly associated with this chemotherapy compound.  Addition of steric bulk cis to the coordinating center of a monofunctional DNA compound is one strategy that has emerged in the development of new chemotherapy drug candidates.  Our results suggest that triamine-ligated complexes with this form of steric bulk can exhibit nuclear compartmental targeting and anti-cancer cell effects competitive with their heterocyclic ligated counterparts.  Further, although the triamine- and heterocyclic ligated complexes produce auditory threshold shifts similar to cisplatin, unlike cisplatin, the monofunctional compounds produce virtually no effect on auditory hair cell density.
  • 13. References  1.Langer T, am Zehnhoff-Dinnesen A, Radtke S, Meitert J, Zolk O. Understanding platinum-induced ototoxicity. Trends Pharmacol Sci. 2013;34: 458–69. pmid:23769626  2.Karasawa T, Steyger PS. An integrated view of cisplatin- induced nephrotoxicity and ototoxicity. Toxicol Lett. 2015;237: 219–27. pmid:26101797  And Cancer Therapy. Cancer. 2016;122: 1647–58. pmid:26859792  4.Lanvers-Kaminsky C, Zehnhoff-Dinnesen AA, Parfitt R, Ciarimboli G. Drug-induced ototoxicity: Mechanisms, Pharmacogenetics, and protective strategies. Clin Pharmacol Ther. 2017;101: 491–500. pmid:28002638