Low thermal evolution degree of gas and connected fracture network are key features in the continental shale gas reservoirs.When the pressure decreases lower than the dew point pressure,gas condensate diminishes the m...Low thermal evolution degree of gas and connected fracture network are key features in the continental shale gas reservoirs.When the pressure decreases lower than the dew point pressure,gas condensate diminishes the mobility of subsurface fluid forms in the near well region,which further reduces the productivity and final recovery factor in addition to the low connected fracture network.This work is motivated to investigate the application of gas injection,proven to be a feasible technique in conventional/marine-shale gas condensate reservoirs,in continental shale gas condensate reservoirs.We apply a compositional model to investigate the mechanism of gas injection treatment taking a continental shale gas condensate reservoir in the Fuxing area,Sichuan Basin,China as an example.The results demonstrate that for the removal of gas condensate during CO_(2)injection,re-vaporization plays the main mechanism through two processes including pressurization and development of miscibility,while the former is overwhelming.Considering the variation trend of the total volume of gas condensate,we divide the whole injection process into four and six stages in the single fracture model and fracture network model,respectively,and reason the trend with respect to phase behavior and flow pattern.A sensitive study on the injected gas type indicates that the sorting of the gas injection performance to remove gas condensate produced gas followed by CH4,and followed by CO_(2).Finally,we investigate the performance of cyclic produced-gas injection and optimize the injection scheme.This work provides technical and theoretical support for the development of continental shale gas reservoirs.展开更多
The goal of the present study is to elucidate the intragastrointestinal fate of micellar delivery systems by monitoring fluorescently labeled different micelles and the model drug paclitaxel(PTX).Both in vitro and ex ...The goal of the present study is to elucidate the intragastrointestinal fate of micellar delivery systems by monitoring fluorescently labeled different micelles and the model drug paclitaxel(PTX).Both in vitro and ex vivo leakage studies showed fast PTX release in fluids while micelles remained intact,except in fedstate simulated intestinal fluid and fasted-state pig intestinal fluid,thus referring to the intact absorption of micelles and PTX leakage in the gastrointestinal tract with D-a-tocopherol polyethylene glycol 1000 succinate(TPGS)micelles showing higher stability than other micelles.All groups of micelles were absorbed intact in Caco-2 and Caco-2/HT29-MTX cell models and the absorption of TPGS micelles was found to be higher than other micelles.The transport of the micelles across Caco-2/Raji(1.6%-3.5%),Caco-2(0.8%-1%),and Caco-2/HT29-MTX(0.58%-1%)cell monolayers further verified the absorption of micelles and their subsequent transport;however,more TPGS micelles transported across cell monolayers than other groups.Moreover,the histological examination also confirmed that micelles ente red the enterocytes and were transported to basolateral tissues and TPGS showed the stronger ability of penetration than other groups.Thus,these results are succinctly presenting the absorption of intact micelles in GIT confirmed by imaging evidence with prior leakage of the drug,upta ke by enterocytes and the transport of micelles that survive the digestion by enterocytes and mainly by microfold cells in material nature dependent way with TPGS showing better results than other groups.In conclusion,these results identify the mechanism by which the gastrointestinal tract processes micelles and point to the likely use of this approach in the design of micelles-based therapies.展开更多
The long-circulating effect is revisited by simultaneous monitoring of the drug payloads and nanocarriers following intravenous administration of doxorubicin(DOX)-loaded methoxy polyethylene glycol-polycaprolactone(mP...The long-circulating effect is revisited by simultaneous monitoring of the drug payloads and nanocarriers following intravenous administration of doxorubicin(DOX)-loaded methoxy polyethylene glycol-polycaprolactone(mPEG-PCL) nanoparticles. Comparison of the kinetic profiles of both DOX and nanocarriers verifies the long-circulating effect, though of limited degree, as a result of pegylation. The nanocarrier profiles display fast clearance from the blood despite dense PEG decoration;DOX is cleared faster than the nanocarriers. The nanocarriers circulate longer than DOX in the blood, suggesting possible leakage of DOX from the nanocarriers. Hepatic accumulation is the highest among all organs and tissues investigated, which however is reversely proportionate to blood circulation time. Pegylation and reduction in particle size prove to extend circulation of drug nanocarriers in the blood with simultaneous decrease in uptake by various organs of the mononuclear phagocytic system. It is concluded that the long-circulating effect of mPEG-PCL nanoparticles is reconfirmed by monitoring of either DOX or the nanocarriers, but the faster clearance of DOX suggests possible leakage of a fraction of the payloads. The findings of this study are of potential translational significance in design of nanocarriers towards optimization of both therapeutic and toxic effects.展开更多
基金supported by the Sinopec Key Laboratory of Shale Oil and Gas Drilling,Completion and Fracturing(Grant No.35800000-22-ZC0613-0023)Beijing Municipal Natural Science Foundation(Grant No.2232073)the Sinopec Science and Technology Department(Grant Nos.P21078-8 and P22005).
文摘Low thermal evolution degree of gas and connected fracture network are key features in the continental shale gas reservoirs.When the pressure decreases lower than the dew point pressure,gas condensate diminishes the mobility of subsurface fluid forms in the near well region,which further reduces the productivity and final recovery factor in addition to the low connected fracture network.This work is motivated to investigate the application of gas injection,proven to be a feasible technique in conventional/marine-shale gas condensate reservoirs,in continental shale gas condensate reservoirs.We apply a compositional model to investigate the mechanism of gas injection treatment taking a continental shale gas condensate reservoir in the Fuxing area,Sichuan Basin,China as an example.The results demonstrate that for the removal of gas condensate during CO_(2)injection,re-vaporization plays the main mechanism through two processes including pressurization and development of miscibility,while the former is overwhelming.Considering the variation trend of the total volume of gas condensate,we divide the whole injection process into four and six stages in the single fracture model and fracture network model,respectively,and reason the trend with respect to phase behavior and flow pattern.A sensitive study on the injected gas type indicates that the sorting of the gas injection performance to remove gas condensate produced gas followed by CH4,and followed by CO_(2).Finally,we investigate the performance of cyclic produced-gas injection and optimize the injection scheme.This work provides technical and theoretical support for the development of continental shale gas reservoirs.
基金supported by the National Natural Science Foundation of China(Nos.81872815,81872826,82030107,81690263)Science and Technology Commission of Shanghai Municipality(No.19XD1400300)。
文摘The goal of the present study is to elucidate the intragastrointestinal fate of micellar delivery systems by monitoring fluorescently labeled different micelles and the model drug paclitaxel(PTX).Both in vitro and ex vivo leakage studies showed fast PTX release in fluids while micelles remained intact,except in fedstate simulated intestinal fluid and fasted-state pig intestinal fluid,thus referring to the intact absorption of micelles and PTX leakage in the gastrointestinal tract with D-a-tocopherol polyethylene glycol 1000 succinate(TPGS)micelles showing higher stability than other micelles.All groups of micelles were absorbed intact in Caco-2 and Caco-2/HT29-MTX cell models and the absorption of TPGS micelles was found to be higher than other micelles.The transport of the micelles across Caco-2/Raji(1.6%-3.5%),Caco-2(0.8%-1%),and Caco-2/HT29-MTX(0.58%-1%)cell monolayers further verified the absorption of micelles and their subsequent transport;however,more TPGS micelles transported across cell monolayers than other groups.Moreover,the histological examination also confirmed that micelles ente red the enterocytes and were transported to basolateral tissues and TPGS showed the stronger ability of penetration than other groups.Thus,these results are succinctly presenting the absorption of intact micelles in GIT confirmed by imaging evidence with prior leakage of the drug,upta ke by enterocytes and the transport of micelles that survive the digestion by enterocytes and mainly by microfold cells in material nature dependent way with TPGS showing better results than other groups.In conclusion,these results identify the mechanism by which the gastrointestinal tract processes micelles and point to the likely use of this approach in the design of micelles-based therapies.
基金supported by the National Natural Science Foundation of China(Nos.81872815,82030107,and 81690263)Science and Technology Commission of Shanghai Municipality(No.19XD1400300,China)。
文摘The long-circulating effect is revisited by simultaneous monitoring of the drug payloads and nanocarriers following intravenous administration of doxorubicin(DOX)-loaded methoxy polyethylene glycol-polycaprolactone(mPEG-PCL) nanoparticles. Comparison of the kinetic profiles of both DOX and nanocarriers verifies the long-circulating effect, though of limited degree, as a result of pegylation. The nanocarrier profiles display fast clearance from the blood despite dense PEG decoration;DOX is cleared faster than the nanocarriers. The nanocarriers circulate longer than DOX in the blood, suggesting possible leakage of DOX from the nanocarriers. Hepatic accumulation is the highest among all organs and tissues investigated, which however is reversely proportionate to blood circulation time. Pegylation and reduction in particle size prove to extend circulation of drug nanocarriers in the blood with simultaneous decrease in uptake by various organs of the mononuclear phagocytic system. It is concluded that the long-circulating effect of mPEG-PCL nanoparticles is reconfirmed by monitoring of either DOX or the nanocarriers, but the faster clearance of DOX suggests possible leakage of a fraction of the payloads. The findings of this study are of potential translational significance in design of nanocarriers towards optimization of both therapeutic and toxic effects.
