Intraperitoneal chemotherapy of ovarian cancer by hydrogel depot of paclitaxel nanocrystals

Bo Sun; Maie S. Taha; Benjamin Ramsey; Sandra Torregrosa-Allen; Bennett D. Elzey; Yoon Yeo

doi:10.1016/j.jconrel.2016.05.056

Intraperitoneal chemotherapy of ovarian cancer by hydrogel depot of paclitaxel nanocrystals

Bo Sun, Maie S. Taha, Benjamin Ramsey, Sandra Torregrosa-Allen, Bennett D. Elzey, Yoon Yeo

Research output: Contribution to journal › Article › peer-review

49 Scopus citations

Abstract

Intraperitoneal (IP) chemotherapy is a promising post-surgical therapy of ovarian cancer, but the full potential is yet to be realized. To facilitate IP chemotherapy of ovarian cancer, we developed an in-situ crosslinkable hydrogel depot containing paclitaxel (PTX) nanocrystals (PNC). PNC suppressed SKOV3 cell proliferation more efficiently than microparticulate PTX precipitates (PPT), and the gel containing PNC (PNC-gel) showed a lower maximum tolerated dose than PPT-containing gel (PPT-gel) in mice, indicating greater dissolution and cellular uptake of PNC than PPT. A single IP administration of PNC-gel extended the survival of tumor-bearing mice significantly better than Taxol, but PPT-gel did not. These results support the advantage of PNC over PPT and demonstrate the promise of a gel depot as an IP drug delivery system.

Original language	English (US)
Pages (from-to)	91-98
Number of pages	8
Journal	Journal of Controlled Release
Volume	235
DOIs	https://doi.org/10.1016/j.jconrel.2016.05.056
State	Published - Aug 10 2016
Externally published	Yes

Keywords

Drug delivery
Hydrogel depot
Intraperitoneal chemotherapy
Nanocrystals
Ovarian cancer

ASJC Scopus subject areas

Pharmaceutical Science

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10.1016/j.jconrel.2016.05.056

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title = "Intraperitoneal chemotherapy of ovarian cancer by hydrogel depot of paclitaxel nanocrystals",

abstract = "Intraperitoneal (IP) chemotherapy is a promising post-surgical therapy of ovarian cancer, but the full potential is yet to be realized. To facilitate IP chemotherapy of ovarian cancer, we developed an in-situ crosslinkable hydrogel depot containing paclitaxel (PTX) nanocrystals (PNC). PNC suppressed SKOV3 cell proliferation more efficiently than microparticulate PTX precipitates (PPT), and the gel containing PNC (PNC-gel) showed a lower maximum tolerated dose than PPT-containing gel (PPT-gel) in mice, indicating greater dissolution and cellular uptake of PNC than PPT. A single IP administration of PNC-gel extended the survival of tumor-bearing mice significantly better than Taxol, but PPT-gel did not. These results support the advantage of PNC over PPT and demonstrate the promise of a gel depot as an IP drug delivery system.",

keywords = "Drug delivery, Hydrogel depot, Intraperitoneal chemotherapy, Nanocrystals, Ovarian cancer",

author = "Bo Sun and Taha, {Maie S.} and Benjamin Ramsey and Sandra Torregrosa-Allen and Elzey, {Bennett D.} and Yoon Yeo",

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year = "2016",

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doi = "10.1016/j.jconrel.2016.05.056",

language = "English (US)",

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T1 - Intraperitoneal chemotherapy of ovarian cancer by hydrogel depot of paclitaxel nanocrystals

AU - Sun, Bo

AU - Taha, Maie S.

AU - Ramsey, Benjamin

AU - Torregrosa-Allen, Sandra

AU - Elzey, Bennett D.

AU - Yeo, Yoon

PY - 2016/8/10

Y1 - 2016/8/10

N2 - Intraperitoneal (IP) chemotherapy is a promising post-surgical therapy of ovarian cancer, but the full potential is yet to be realized. To facilitate IP chemotherapy of ovarian cancer, we developed an in-situ crosslinkable hydrogel depot containing paclitaxel (PTX) nanocrystals (PNC). PNC suppressed SKOV3 cell proliferation more efficiently than microparticulate PTX precipitates (PPT), and the gel containing PNC (PNC-gel) showed a lower maximum tolerated dose than PPT-containing gel (PPT-gel) in mice, indicating greater dissolution and cellular uptake of PNC than PPT. A single IP administration of PNC-gel extended the survival of tumor-bearing mice significantly better than Taxol, but PPT-gel did not. These results support the advantage of PNC over PPT and demonstrate the promise of a gel depot as an IP drug delivery system.

AB - Intraperitoneal (IP) chemotherapy is a promising post-surgical therapy of ovarian cancer, but the full potential is yet to be realized. To facilitate IP chemotherapy of ovarian cancer, we developed an in-situ crosslinkable hydrogel depot containing paclitaxel (PTX) nanocrystals (PNC). PNC suppressed SKOV3 cell proliferation more efficiently than microparticulate PTX precipitates (PPT), and the gel containing PNC (PNC-gel) showed a lower maximum tolerated dose than PPT-containing gel (PPT-gel) in mice, indicating greater dissolution and cellular uptake of PNC than PPT. A single IP administration of PNC-gel extended the survival of tumor-bearing mice significantly better than Taxol, but PPT-gel did not. These results support the advantage of PNC over PPT and demonstrate the promise of a gel depot as an IP drug delivery system.

KW - Drug delivery

KW - Hydrogel depot

KW - Intraperitoneal chemotherapy

KW - Nanocrystals

KW - Ovarian cancer

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SN - 0168-3659

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SP - 91

EP - 98

JO - Journal of Controlled Release

JF - Journal of Controlled Release

ER -

Intraperitoneal chemotherapy of ovarian cancer by hydrogel depot of paclitaxel nanocrystals

Abstract

Keywords

ASJC Scopus subject areas

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