TY - JOUR
T1 - Novel therapeutic strategy for prevention of malignant tumor recurrence after surgery
T2 - Local delivery and prolonged release of adenovirus immobilized in photocured, tissue-adhesive gelatinous matrix
AU - Okino, Hidenobu
AU - Manabe, Tatsuya
AU - Tanaka, Masao
AU - Matsuda, Takehisa
PY - 2003/9/1
Y1 - 2003/9/1
N2 - We have been developing a new gene delivery method using a styrenated gelatin-based tissue-adhesive matrix that allows in situ adenovirus-immobilized gel formation on living tissue and sustained virus release to permeate carcinoma tissue. Styrenated gelatin was synthesized by the condensation reaction of gelatin with 4-vinylbenzoic acid. Aqueous styrenated gelatin solution premixed with AdLacZ, adenovirus encoding β-galactosidase cDNA, and carboxylated camphorquinone (CQ) as a photoinitiator was irradiated with visible light to form a styrenated gelatin gel. The in vitro adenovirus release from the styrenated gelatin gel to a medium strongly depended not on styrenated gelatin concentration but on CQ concentration. Maximal β-galactosidase expression was observed on day 1, followed bv a rapid decrease that continued up to 1 month for a styrenated gelatin gel prepared with a low styrenated gelatin concentration and a low CQ concentration. Dose-dependent reduced expression of β-galactosidase activity with increasing CQ under photoirradiation was observed. AdLacZ-immobilized styrenated gelatin gel was formed on a hybrid tissue, which is a cell traction-induced collagenous gel entrapped with fibroblasts, and lacZ gene expression of fibroblasts in the hybrid tissue was observed for more than one month. The result of this in vitro model experiment implies that the tissue-adhesive styrenated gelatin may be applicable for the delivery of adenovirus encoding cDNA for tumor dormancy therapy into malignant tissue to prevent tumor recurrence after surgery when CDNA is properly selected.
AB - We have been developing a new gene delivery method using a styrenated gelatin-based tissue-adhesive matrix that allows in situ adenovirus-immobilized gel formation on living tissue and sustained virus release to permeate carcinoma tissue. Styrenated gelatin was synthesized by the condensation reaction of gelatin with 4-vinylbenzoic acid. Aqueous styrenated gelatin solution premixed with AdLacZ, adenovirus encoding β-galactosidase cDNA, and carboxylated camphorquinone (CQ) as a photoinitiator was irradiated with visible light to form a styrenated gelatin gel. The in vitro adenovirus release from the styrenated gelatin gel to a medium strongly depended not on styrenated gelatin concentration but on CQ concentration. Maximal β-galactosidase expression was observed on day 1, followed bv a rapid decrease that continued up to 1 month for a styrenated gelatin gel prepared with a low styrenated gelatin concentration and a low CQ concentration. Dose-dependent reduced expression of β-galactosidase activity with increasing CQ under photoirradiation was observed. AdLacZ-immobilized styrenated gelatin gel was formed on a hybrid tissue, which is a cell traction-induced collagenous gel entrapped with fibroblasts, and lacZ gene expression of fibroblasts in the hybrid tissue was observed for more than one month. The result of this in vitro model experiment implies that the tissue-adhesive styrenated gelatin may be applicable for the delivery of adenovirus encoding cDNA for tumor dormancy therapy into malignant tissue to prevent tumor recurrence after surgery when CDNA is properly selected.
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U2 - 10.1002/jbm.a.10016
DO - 10.1002/jbm.a.10016
M3 - Article
C2 - 12918048
AN - SCOPUS:0345168906
SN - 0021-9304
VL - 66
SP - 643
EP - 651
JO - Journal of Biomedical Materials Research - Part A
JF - Journal of Biomedical Materials Research - Part A
IS - 3
ER -