2009
DOI: 10.1016/j.biomaterials.2009.05.031
|View full text |Cite
|
Sign up to set email alerts
|

Doxorubicin–polyphosphazene conjugate hydrogels for locally controlled delivery of cancer therapeutics

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
59
0

Year Published

2011
2011
2022
2022

Publication Types

Select...
7
2
1

Relationship

0
10

Authors

Journals

citations
Cited by 117 publications
(60 citation statements)
references
References 38 publications
1
59
0
Order By: Relevance
“…Over more than 20 days, the release rate of doxorubicin was successfully controlled by altering the mechanical strength of polyphosphazene. Later, Song and colleagues exploited a conjugation strategy involving doxorubicin and paclitaxel as therapeutic agents coupled to a polyphophazene backbone for local tumor treatment [94,95]. Another method of conjugation in polyphosphazene hydrogels involves a modification with protamine or poly-L-arginine for the delivery of human growth hormone (hGH) [96], which results in poly-L-arginine-or protamine-modified poplyphosphazene releasing hGH for up to 5 days in vivo or 7 days in vitro, respectively.…”
Section: Temperature Sensitive Hydrogelsmentioning
confidence: 98%
“…Over more than 20 days, the release rate of doxorubicin was successfully controlled by altering the mechanical strength of polyphosphazene. Later, Song and colleagues exploited a conjugation strategy involving doxorubicin and paclitaxel as therapeutic agents coupled to a polyphophazene backbone for local tumor treatment [94,95]. Another method of conjugation in polyphosphazene hydrogels involves a modification with protamine or poly-L-arginine for the delivery of human growth hormone (hGH) [96], which results in poly-L-arginine-or protamine-modified poplyphosphazene releasing hGH for up to 5 days in vivo or 7 days in vitro, respectively.…”
Section: Temperature Sensitive Hydrogelsmentioning
confidence: 98%
“…It was observed that the toxicity of DOX was reduced in conjugated form. [33] Kholar et al [34] immobilized the methotrexate on dextran-coated iron oxide nanoparticles and provided evidence that the drug loading on such nanoparticles was possible due to electrostatic interaction between the positively charged methotrexate and negatively charged polymer layer on nanoparticles. It was observed that the change in pH is sufficient to release the medicine from nanoparticles.…”
Section: Discussionmentioning
confidence: 97%
“…Consequently, thermal and mechanical properties of PPZ greatly vary with T g ranging from −10 to 35 °C, contact angle 63°-107°, tensile strength 2.4-7.6 MPa, and modulus of elasticity 31.4-455.9 MPa [264]. PPZ are fabricated into particles, micelles, microneedle coatings, and gels for the delivery of anti-inflammatory drugs, chemotherapeutics, growth factors, DNA, proteins, and vaccines [265][266][267][268]. Moreover, PPZ scaffolds composed of films, fibers, and microspheres are used to assist nerve regeneration and orthopedic applications, alone or blended with polyesters to increase mechanical strength and provide a moderate pH microenvironment for developing tissues [269][270][271].…”
Section: Polyphosphazenesmentioning
confidence: 99%