Dynamic Ureas with Fast and pH-Independent Hydrolytic Kinetics.

Low cost, high performance hydrolysable polymers are of great importance in biomedical applications and materials industries. While many applications require materials to have a degradation profile insensitive to external pH to achieve consistent release profiles under varying conditions, hydrolysable chemistry techniques developed so far have pH-dependent hydrolytic kinetics. This work reports the design and synthesis of a new type of hydrolysable polymer that has identical hydrolysis kinetics from pH 3 to 11. The unprecedented pH independent hydrolytic kinetics of the aryl ureas were shown to be related to the dynamic bond dissociation controlled hydrolysis mechanism; the resulting hindered poly(aryl urea) can be degraded with a hydrolysis half-life of 10 min in solution. More importantly, these fast degradable hindered aromatic polyureas can be easily prepared by addition polymerization from commercially available monomers and are resistant to hydrolysis in solid form for months under ambient storage conditions. The combined features of good stability in solid state and fast hydrolysis at various pH values is unprecedented in polyurea material, and will have implications for materials design and applications, such as sacrificial coatings and biomaterials.

[1]  Yan Zhang,et al.  Enhanced bioreduction-responsive biodegradable diselenide-containing poly(ester urethane) nanocarriers. , 2017, Biomaterials science.

[2]  C. Breuer,et al.  Pilot Mouse Study of 1 mm Inner Diameter (ID) Vascular Graft Using Electrospun Poly(ester urea) Nanofibers , 2016, Advanced healthcare materials.

[3]  M. Delius,et al.  The Dynamic Covalent Chemistry of Esters, Acetals and Orthoesters , 2016 .

[4]  M. Becker,et al.  Caddisfly Inspired Phosphorylated Poly(ester urea)-Based Degradable Bone Adhesives. , 2016, Biomacromolecules.

[5]  L. Dobrucki,et al.  Pamidronate functionalized nanoconjugates for targeted therapy of focal skeletal malignant osteolysis , 2016, Proceedings of the National Academy of Sciences.

[6]  Yi Yan Yang,et al.  Broad‐Spectrum Antimicrobial Star Polycarbonates Functionalized with Mannose for Targeting Bacteria Residing inside Immune Cells , 2016, Advanced healthcare materials.

[7]  L. Tang,et al.  Targeted Delivery of Immunomodulators to Lymph Nodes , 2016, Cell reports.

[8]  K. Fukushima,et al.  Poly(trimethylene carbonate)-based polymers engineered for biodegradable functional biomaterials. , 2016, Biomaterials science.

[9]  Ruairí P. Brannigan,et al.  Synthesis, properties and biomedical applications of hydrolytically degradable materials based on aliphatic polyesters and polycarbonates. , 2016, Biomaterials science.

[10]  M. Repka,et al.  Formulation and development of pH-independent/dependent sustained release matrix tablets of ondansetron HCl by a continuous twin-screw melt granulation process. , 2015, International journal of pharmaceutics.

[11]  G. Alobaidi,et al.  Optimization of pH-independent chronotherapeutic release of verapamil HCl from three-layer matrix tablets. , 2015, International journal of pharmaceutics.

[12]  Yi Yan Yang,et al.  Biodegradable Antimicrobial Polycarbonates with In Vivo Efficacy against Multidrug‐Resistant MRSA Systemic Infection , 2015, Advanced healthcare materials.

[13]  Lichen Yin,et al.  Synthesis and biomedical applications of functional poly(α-hydroxy acids) via ring-opening polymerization of O-carboxyanhydrides. , 2015, Accounts of chemical research.

[14]  Zhibin Guan,et al.  Malleable and Self-Healing Covalent Polymer Networks through Tunable Dynamic Boronic Ester Bonds. , 2015, Journal of the American Chemical Society.

[15]  Jeffery E. Raymond,et al.  Improving paclitaxel delivery: in vitro and in vivo characterization of PEGylated polyphosphoester-based nanocarriers. , 2015, Journal of the American Chemical Society.

[16]  Haotian Sun,et al.  A degradable brush polymer-drug conjugate for pH-responsive release of doxorubicin , 2015 .

[17]  W. Phillip,et al.  Synthesis of degradable molecular brushes via a combination of ring‐opening polymerization and click chemistry , 2015 .

[18]  Jianjun Cheng,et al.  Hydrolyzable Polyureas Bearing Hindered Urea Bonds , 2014, Journal of the American Chemical Society.

[19]  J. Feijen,et al.  Advanced drug and gene delivery systems based on functional biodegradable polycarbonates and copolymers. , 2014, Journal of controlled release : official journal of the Controlled Release Society.

[20]  Yi Yan Yang,et al.  Injectable Hydrogels from Triblock Copolymers of Vitamin E‐Functionalized Polycarbonate and Poly(ethylene glycol) for Subcutaneous Delivery of Antibodies for Cancer Therapy , 2014 .

[21]  Jianjun Cheng,et al.  Dynamic urea bond for the design of reversible and self-healing polymers , 2014, Nature Communications.

[22]  S. K. Li,et al.  Silicone Adhesive Matrix of Verapamil Hydrochloride to Provide pH-Independent Sustained Release , 2014, AAPS PharmSciTech.

[23]  K. Wooley,et al.  Construction of a Reactive Diblock Copolymer, Polyphosphoester-block-Poly(L-lactide), as a Versatile Framework for Functional Materials that are Capable of Full Degradation and Nanoscopic Assembly Formation. , 2013, ACS macro letters.

[24]  Sei-Hum Jang,et al.  pH-dependent, thermosensitive polymeric nanocarriers for drug delivery to solid tumors. , 2013, Biomaterials.

[25]  Amolkumar Karwa,et al.  Poly(ethylene oxide)-block-polyphosphester-based Paclitaxel Conjugates as a Platform for Ultra-high Paclitaxel-loaded Multifunctional Nanoparticles. , 2013, Chemical science.

[26]  J. F. Stoddart,et al.  Dynamic imine chemistry. , 2012, Chemical Society reviews.

[27]  Paula T. Hammond,et al.  Mixed micelles self-assembled from block copolymers for drug delivery , 2011 .

[28]  A. Albertsson,et al.  Degradable polyethylene: fantasy or reality. , 2011, Environmental science & technology.

[29]  G. Kaur,et al.  pH modulation: a mechanism to obtain pH-independent drug release , 2010, Expert opinion on drug delivery.

[30]  Neeraj Kumar,et al.  Polyanhydrides as localized drug delivery carrier: an update , 2008 .

[31]  S. Standley,et al.  Fully acid-degradable biocompatible polyacetal microparticles for drug delivery. , 2008, Bioconjugate chemistry.

[32]  Jean M. J. Fréchet,et al.  Synthesis and Degradation of pH-Sensitive Linear Poly(amidoamine)s , 2007 .

[33]  Y. Tsai,et al.  Optimization of pH-independent release of nicardipine hydrochloride extended-release matrix tablets using response surface methodology. , 2005, International journal of pharmaceutics.

[34]  Jorge Heller,et al.  Poly(ortho esters)--from concept to reality. , 2004, Biomacromolecules.

[35]  S. Brocchini,et al.  Polyacetal-doxorubicin conjugates designed for pH-dependent degradation. , 2003, Bioconjugate chemistry.

[36]  Abraham J Domb,et al.  Polyanhydrides: an overview. , 2002, Advanced drug delivery reviews.

[37]  Robert Gurny,et al.  Poly(ortho esters): synthesis, characterization, properties and uses. , 2002, Advanced drug delivery reviews.

[38]  Randhir Singh,et al.  Intramolecular general base catalyzed ester hydrolysis. The hydrolysis of 2-aminobenzoate esters. , 2002, The Journal of organic chemistry.

[39]  A. J. Bennet,et al.  Cyclodextrin catalysis of the pH-independent hydrolyses of acetals , 2001 .

[40]  R. A. Jain,et al.  The manufacturing techniques of various drug loaded biodegradable poly(lactide-co-glycolide) (PLGA) devices. , 2000, Biomaterials.

[41]  E. Castro,et al.  The kinetics of hydrolysis of methyl and phenyl lsocyanates , 1985 .

[42]  M. Sinnott,et al.  Generation of glycopyranosyl cations in the spontaneous hydrolyses of 2,4-dinitrophenyl glycopyranosides. Evidence for the general intermediacy of glycopyranosyl cations in the acid-catalysed hydrolyses of methyl glycopyranosides , 1975 .

[43]  T. Fife,et al.  General acid catalysis and the pH-independent hydrolysis of 2-(p-nitrophenoxy) tetrahydropyran , 1970 .

[44]  P. Mader Hydrolysis kinetics for p-dimethylaminophenyl isocyanate in aqueous solutions , 1968 .