| Project/Area Number |
07671765
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Obstetrics and gynecology
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| Research Institution | University of Tsukuba |
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Principal Investigator |
NISHIDA Masato University of Tsukuba, Assistant Professor, 臨床医学系, 講師 (00110875)
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| Co-Investigator(Kenkyū-buntansha) |
TSUNODA Hajime University of Tsukuba, Assistant Professor, 臨床医学系, 講師 (60197754)
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1996: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1995: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | cancer cells / tissue culture / transplantation / alginate microcapsule / anti-tumor agents / chemosensitivity test / uterine cancer / ovarian cancer / 抗癌剤感受性試験 / マイクロカプセル |
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| Research Abstract |
Low molecular weight substances such as glucose can pass through the membrane composed of polylysine and alginate, but the high molecular weight substances such as immunoglobulin can not pass through this membrane. Therefore, microencapsulation of living cells can protect heterotransplanted cells from rejection. This research aims to establish a new chemosensitivity test system using microencapsulated human cancer cells transplanted into mouse in vivo.
1.Cell encapsulation
The microcapsules were produced according to the procedure originally reported by Lin, using the Ishikawa cells (an established endometrial adenocarcinoma cell line) for encapsulated cells. Cells were suspended in sodium alginate at a concentration of 1x10^6/ml. This cell suspension formed gelled spherical microdroplets by atomizing into CaCl_2 After coated with polylysine, the gels were washed with sodium alginate and CaCl_2 again. Further washing was employed with sodium citrate to liquify the gel inside the capsules. The adequate size of the capsules with a membrane of polylysine sandwiched between 2 layrs of alginate were 0.5 mm in diameter for manipulation.
After several trials and errors, the microcapsules could be produced smoothly.
2.Cultivation of the microcapsules in vitro
The capsules were suspended in the culture media and cultured under the closed condition.
The phasecontrast microscopic findings revealed that the solitary cancer cells in its early stage grow rapidly foaming aggregates in the microcapsules. The growth curves of the encapsulated cells assessed by SDI analysis showed exponential growth of the cells.
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