PH‐Sensitive Drug‐Conjugates on Water‐Soluble Polymer Frameworks. Issue 3 (20th November 2014)
- Record Type:
- Journal Article
- Title:
- PH‐Sensitive Drug‐Conjugates on Water‐Soluble Polymer Frameworks. Issue 3 (20th November 2014)
- Main Title:
- PH‐Sensitive Drug‐Conjugates on Water‐Soluble Polymer Frameworks
- Authors:
- Siddique, Abu Bakkar
Cho, Youngjun
Kim, Yujin
Bahng, Sung Hoon
Kim, Sung Woo
Lee, Jae Yeol
Kang, Ho‐Jung
Kim, Sehoon
Bae, You Han
Kim, Jungahn - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A potent synthetic methodology is introduced to generate a useful intermediate for the preparation of 'smart' polymeric pro‐drugs. Herein, living anionic block polymerization of ethylene oxide (EO) and <italic>N</italic>‐phenylmaleimide (<italic>N</italic>‐PMI), as well as the Gabriel process, are introduced. Hydrazinolysis of the resulting poly(ethylene oxide)‐<italic>block</italic>‐poly(<italic>N</italic>‐PMI) (PEO‐<italic>b</italic>‐P<italic>N</italic>‐PMI) using hydrazine under acidic conditions leads to the production of PEO‐based frameworks with hydrazide (HZ) groups. The HZ groups are found to effect the formation of an acid‐sensitive bond in reactions with medicines or drugs under neutral conditions (pH 7.2). The PEO‐HZ intermediate, which shows a strong triplet splitting patterned chemical shift in the range <italic>δ</italic> = 6.5–8.5 ppm, represents the most powerful material employed for mass production of smart polymeric pro‐drugs while controlling the drug‐loading yield. Water‐soluble "smart" polymeric pro‐drugs, such as poly(ethylene oxide)‐doxorubicin (PEO‐HZ‐Dox), poly(ethylene oxide)‐methotrexate (PEO‐HZ‐MTX), and poly(ethylene oxide)‐folate (PEO‐HZ‐FA) conjugates, show excellent acid‐sensitive release profiles in water or alcohol at pH 4.5. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor"<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A potent synthetic methodology is introduced to generate a useful intermediate for the preparation of 'smart' polymeric pro‐drugs. Herein, living anionic block polymerization of ethylene oxide (EO) and <italic>N</italic>‐phenylmaleimide (<italic>N</italic>‐PMI), as well as the Gabriel process, are introduced. Hydrazinolysis of the resulting poly(ethylene oxide)‐<italic>block</italic>‐poly(<italic>N</italic>‐PMI) (PEO‐<italic>b</italic>‐P<italic>N</italic>‐PMI) using hydrazine under acidic conditions leads to the production of PEO‐based frameworks with hydrazide (HZ) groups. The HZ groups are found to effect the formation of an acid‐sensitive bond in reactions with medicines or drugs under neutral conditions (pH 7.2). The PEO‐HZ intermediate, which shows a strong triplet splitting patterned chemical shift in the range <italic>δ</italic> = 6.5–8.5 ppm, represents the most powerful material employed for mass production of smart polymeric pro‐drugs while controlling the drug‐loading yield. Water‐soluble "smart" polymeric pro‐drugs, such as poly(ethylene oxide)‐doxorubicin (PEO‐HZ‐Dox), poly(ethylene oxide)‐methotrexate (PEO‐HZ‐MTX), and poly(ethylene oxide)‐folate (PEO‐HZ‐FA) conjugates, show excellent acid‐sensitive release profiles in water or alcohol at pH 4.5. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh3pgjp8b6" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract> … (more)
- Is Part Of:
- Macromolecular chemistry and physics. Volume 216:Issue 3(2015:Feb.)
- Journal:
- Macromolecular chemistry and physics
- Issue:
- Volume 216:Issue 3(2015:Feb.)
- Issue Display:
- Volume 216, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 216
- Issue:
- 3
- Issue Sort Value:
- 2015-0216-0003-0000
- Page Start:
- 265
- Page End:
- 276
- Publication Date:
- 2014-11-20
- Subjects:
- Polymers -- Periodicals
Polymerization -- Periodicals
Synthetic products -- Periodicals
Macromolecules -- Periodicals
547.7 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/macp.201400457 ↗
- Languages:
- English
- ISSNs:
- 1022-1352
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.398000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4045.xml