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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53472생성일: 2026년 10월 25일

Furan-2,5-dione--methoxyethene (1/1) → 2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)benzoic acid

https://huagongshe.com/reaction/53472

반응식

참여 물질

역할이름HCID투입량
반응물Furan-2,5-dione--methoxyethene (1/1)HCID 62708—
반응물Sodium 3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-3',6'-bis(olate)HCID 9885981—
생성물2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)benzoic acidHCID 3383—

반응 단계

In order to determine the temperature stability and release profile of the nonaqueous drug delivery vehicle suspensions of the present invention microparticulates containing 5% sodium fluorescein were prepared utilizing poly(methylvinylether/maleic anhydride) as the polymer matrix utilizing the manufacturing technique of Example 1 and were suspended in PFD as a 2% w/v suspension utilizing the technique of Example 4. This nonaqueous drug delivery vehicle suspension was divided in half and equal portions were stored at 23° C. and at 45° C. for thirty days. Samples were taken of each portion during the thirty day test period and fluorescein release profiles were obtained as is known in the art. More specifically, the dissolution tests were performed as follows. 500 ml of 7.4 pH phosphate buffer (0.05M) was added to the kettles in the standard USP dissolution apparatus set at 37° C. 10 ml of the 2% w/v suspension was slowly added to the dissolution medium and the propeller speed was set to 50 rpm. Over a seven hour time period, samples were taken from the dissolution medium and immediately centrifuged. The supernatant containing the released fluorescein was assayed for fluorescein content by UV spectrophotometry. Release profiles for the 23° C. and 45° C. samples are given in FIGS. 1 and 2. The control was freshly prepared microparticulates.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620699
출처 데이터셋uspto-grants-1997_04
ORD IDord-61b08e408bf2461a8c371e9bb9eef7b9
출처 메모uspto-grants-1997_04