A pH‐Triggered Polymer Degradation or Drug Delivery System by Light‐Mediated Cis/Trans Isomerization of o‐Hydroxy Cinnamates

A new methodology for the pH‐triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho‐hydroxy‐cinnamates (oHC) to coumarins is described. The key oHC structural motif can be readily incorporated into the rational design of novel...

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Published inMacromolecular rapid communications. Vol. 42; no. 13; pp. e2100213 - n/a
Main Authors Abramov, Alex, Maiti, Binoy, Keridou, Ina, Puiggalí, Jordi, Reiser, Oliver, Díaz, David Díaz
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 01.07.2021
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Abstract A new methodology for the pH‐triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho‐hydroxy‐cinnamates (oHC) to coumarins is described. The key oHC structural motif can be readily incorporated into the rational design of novel photocleavable polymers via click chemistry. This main‐chain moiety undergoes a fast photocleavage when irradiated with 455 nm light provided that a suitable base is added. A series of polyethylene glycol‐alt‐ortho‐hydroxy cinnamate (polyethylene glycol (PEG)n‐alt‐oHC)‐based polymers are synthesized and the time‐dependent visible‐light initiated cleavage of the photoactive monomer and polymer is investigated in solution by a variety of spectroscopic and chromatographic techniques. The photo‐degradation behavior of the water‐soluble poly(PEG2000‐alt‐oHC) is investigated within a broad pH range (pH = 2.1–11.8), demonstrating fast degradation at pH 11.8, while the stability of the polymer is greatly enhanced at pH 2.1. Moreover, the neat polymer shows long‐term stability under daylight conditions, thus allowing its storage without special precautions. In addition, two water‐soluble PEG‐based drug‐carrier molecules (mPEG2000‐oHC‐benzhydrol/phenol) are synthesized and used for drug delivery studies, monitoring the process by UV–vis spectroscopy in an ON/OFF intermittent manner. Coumarins can be rapidly synthesized from trans‐ortho‐hydroxycinnamates under visible light irradiation in the absence of a photocatalyst based on a bathochromic shift of its absorption from the UV to the visible light region under basic conditions. This methodology is applied for the preparation of dual pH‐ and photo‐responsive polymers with potential for degradable polymer and drug delivery applications.
AbstractList A new methodology for the pH‐triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho‐hydroxy‐cinnamates (oHC) to coumarins is described. The key oHC structural motif can be readily incorporated into the rational design of novel photocleavable polymers via click chemistry. This main‐chain moiety undergoes a fast photocleavage when irradiated with 455 nm light provided that a suitable base is added. A series of polyethylene glycol‐alt‐ortho‐hydroxy cinnamate (polyethylene glycol (PEG)n‐alt‐oHC)‐based polymers are synthesized and the time‐dependent visible‐light initiated cleavage of the photoactive monomer and polymer is investigated in solution by a variety of spectroscopic and chromatographic techniques. The photo‐degradation behavior of the water‐soluble poly(PEG2000‐alt‐oHC) is investigated within a broad pH range (pH = 2.1–11.8), demonstrating fast degradation at pH 11.8, while the stability of the polymer is greatly enhanced at pH 2.1. Moreover, the neat polymer shows long‐term stability under daylight conditions, thus allowing its storage without special precautions. In addition, two water‐soluble PEG‐based drug‐carrier molecules (mPEG2000‐oHC‐benzhydrol/phenol) are synthesized and used for drug delivery studies, monitoring the process by UV–vis spectroscopy in an ON/OFF intermittent manner.
A new methodology for the pH‐triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho ‐hydroxy‐cinnamates ( o HC) to coumarins is described. The key o HC structural motif can be readily incorporated into the rational design of novel photocleavable polymers via click chemistry. This main‐chain moiety undergoes a fast photocleavage when irradiated with 455 nm light provided that a suitable base is added. A series of polyethylene glycol‐ alt ‐ ortho ‐hydroxy cinnamate (polyethylene glycol (PEG) n ‐ alt ‐ o HC)‐based polymers are synthesized and the time‐dependent visible‐light initiated cleavage of the photoactive monomer and polymer is investigated in solution by a variety of spectroscopic and chromatographic techniques. The photo‐degradation behavior of the water‐soluble poly(PEG 2000 ‐ alt ‐ o HC) is investigated within a broad pH range (pH = 2.1–11.8), demonstrating fast degradation at pH 11.8, while the stability of the polymer is greatly enhanced at pH 2.1. Moreover, the neat polymer shows long‐term stability under daylight conditions, thus allowing its storage without special precautions. In addition, two water‐soluble PEG‐based drug‐carrier molecules (mPEG 2000 ‐ o HC‐benzhydrol/phenol) are synthesized and used for drug delivery studies, monitoring the process by UV–vis spectroscopy in an ON/OFF intermittent manner.
A new methodology for the pH‐triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho‐hydroxy‐cinnamates (oHC) to coumarins is described. The key oHC structural motif can be readily incorporated into the rational design of novel photocleavable polymers via click chemistry. This main‐chain moiety undergoes a fast photocleavage when irradiated with 455 nm light provided that a suitable base is added. A series of polyethylene glycol‐alt‐ortho‐hydroxy cinnamate (polyethylene glycol (PEG)n‐alt‐oHC)‐based polymers are synthesized and the time‐dependent visible‐light initiated cleavage of the photoactive monomer and polymer is investigated in solution by a variety of spectroscopic and chromatographic techniques. The photo‐degradation behavior of the water‐soluble poly(PEG2000‐alt‐oHC) is investigated within a broad pH range (pH = 2.1–11.8), demonstrating fast degradation at pH 11.8, while the stability of the polymer is greatly enhanced at pH 2.1. Moreover, the neat polymer shows long‐term stability under daylight conditions, thus allowing its storage without special precautions. In addition, two water‐soluble PEG‐based drug‐carrier molecules (mPEG2000‐oHC‐benzhydrol/phenol) are synthesized and used for drug delivery studies, monitoring the process by UV–vis spectroscopy in an ON/OFF intermittent manner. Coumarins can be rapidly synthesized from trans‐ortho‐hydroxycinnamates under visible light irradiation in the absence of a photocatalyst based on a bathochromic shift of its absorption from the UV to the visible light region under basic conditions. This methodology is applied for the preparation of dual pH‐ and photo‐responsive polymers with potential for degradable polymer and drug delivery applications.
A new methodology for the pH-triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho-hydroxy-cinnamates (oHC) to coumarins is described. The key oHC structural motif can be readily incorporated into the rational design of novel photocleavable polymers via click chemistry. This main-chain moiety undergoes a fast photocleavage when irradiated with 455 nm light provided that a suitable base is added. A series of polyethylene glycol-alt-ortho-hydroxy cinnamate (polyethylene glycol (PEG)n -alt-oHC)-based polymers are synthesized and the time-dependent visible-light initiated cleavage of the photoactive monomer and polymer is investigated in solution by a variety of spectroscopic and chromatographic techniques. The photo-degradation behavior of the water-soluble poly(PEG2000 -alt-oHC) is investigated within a broad pH range (pH = 2.1-11.8), demonstrating fast degradation at pH 11.8, while the stability of the polymer is greatly enhanced at pH 2.1. Moreover, the neat polymer shows long-term stability under daylight conditions, thus allowing its storage without special precautions. In addition, two water-soluble PEG-based drug-carrier molecules (mPEG2000 -oHC-benzhydrol/phenol) are synthesized and used for drug delivery studies, monitoring the process by UV-vis spectroscopy in an ON/OFF intermittent manner.A new methodology for the pH-triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho-hydroxy-cinnamates (oHC) to coumarins is described. The key oHC structural motif can be readily incorporated into the rational design of novel photocleavable polymers via click chemistry. This main-chain moiety undergoes a fast photocleavage when irradiated with 455 nm light provided that a suitable base is added. A series of polyethylene glycol-alt-ortho-hydroxy cinnamate (polyethylene glycol (PEG)n -alt-oHC)-based polymers are synthesized and the time-dependent visible-light initiated cleavage of the photoactive monomer and polymer is investigated in solution by a variety of spectroscopic and chromatographic techniques. The photo-degradation behavior of the water-soluble poly(PEG2000 -alt-oHC) is investigated within a broad pH range (pH = 2.1-11.8), demonstrating fast degradation at pH 11.8, while the stability of the polymer is greatly enhanced at pH 2.1. Moreover, the neat polymer shows long-term stability under daylight conditions, thus allowing its storage without special precautions. In addition, two water-soluble PEG-based drug-carrier molecules (mPEG2000 -oHC-benzhydrol/phenol) are synthesized and used for drug delivery studies, monitoring the process by UV-vis spectroscopy in an ON/OFF intermittent manner.
Author Reiser, Oliver
Keridou, Ina
Díaz, David Díaz
Abramov, Alex
Puiggalí, Jordi
Maiti, Binoy
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Snippet A new methodology for the pH‐triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of...
A new methodology for the pH‐triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of ortho...
A new methodology for the pH-triggered degradation of polymers or for the release of drugs under visible light irradiation based on the cyclization of...
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StartPage e2100213
SubjectTerms Chemical synthesis
Chromatography
coumarins
Degradation
Drug delivery
Drug delivery systems
E/Z‐double bond isomerization
Irradiation
Isomerization
Light irradiation
o‐hydroxy cinnamates
pH effects
Phenols
Polyethylene glycol
polymer degradation
Polymers
Spectroscopy
Stability
visible light photocatalysis
Title A pH‐Triggered Polymer Degradation or Drug Delivery System by Light‐Mediated Cis/Trans Isomerization of o‐Hydroxy Cinnamates
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmarc.202100213
https://www.proquest.com/docview/2549040230
https://www.proquest.com/docview/2532247596
Volume 42
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