Search

The thermal reservoir in Taiyun area mainly consists of Ordovician and Cambrian carbonate formations. The target interval of example well contains more than 95% carbonate, being thick, argilliferous and have well-developed natural fissures and rich hot water. However, sometimes stimulation is necessary to achieve the designed water production rate. In this paper, multistage alternating injection acid fracturing technology is selected according to lithologic characteristics of geothermal reservoir. A gel acid, which is a composite of 20%HCl+0.8%SHY1+2% corrosion inhibitor+1.5% iron ion stabilizer+1% cleanup additive, is optimized and developed by experimental tests. Its viscosity can reach 27 mPa·s. Then, pumping schedule of multi-stage alternate injection acid fracturing is optimized by numerical simulator of acid fracturing design. It is shown from job pressure of field sample well that resistance reduction ability of gel acid needs to be further improved. Moreover, from the analysis results of pressure decline after acid fracturing, the fluid efficiency is 42.32%, net pressure is 3.3 MPa, and the dynamic fracture length is 107m, the maximum fracture width is 8.6mm by fitting treatment pressure. The water production increase factor reaches 1.2 after acid fracturing treatment. Therefore, the acid fracturing treatment is successful.

Herein an Ir(III) complex [Ir(Hppy)2(HMNPIP)](PF6) (Ir1, Hppy = 2-phenylpyridine, HMNPIP = 2-(1H-imidazo[4,5-f][1, 10]phenanthroline-3-yl)-6-methoxy-4-nitrophenol) was prepared and characterized. Due to the low anticancer activity of Ir1 when administered free drug, we prepared a liposome Ir1Lipo encapsulated form of Ir1 to improve the antitumor effect, furthermore, we explored the antitumor mechanism of both forms in vitro experiments on HepG2 cells. We investigated the inhibitory efficiency of Ir1 and Ir1Lipo on cell viability and proliferation using MTT (MTT = 3-(4,5-dimethylthiazole)-2,5-diphenltetraazolium bromide) and colony-forming assay. Intracellular accumulation of reactive oxygen species (ROS) was examined using a fluorescence microscope (High Content Screening System, ImageXpress Micro XLS System, Molecular Devices LLC, Sunnyvale, CA), programmed cell death cells stained with acridine orange/ethidium bromide (AO/EB) using flow cytometry detection and western blot have been performed. An in vivo study where HepG2 cells were transplanted into nude nice as xenografts. Tumour volume and body weight were monitored during the 10 days of administration. After encapsulation in liposomes Ir1Lipo displayed high potency against a variety of tumour cells in vitro, especially against HepG2 (IC50 = 4.6 ± 0.5 μM). Mechanism studies indicated that Ir1Lipo initiated apoptosis by generating intracellular ROS that regulate lysosomal-mitochondrial dysfunction, followed by microtubule disruption that subsequently leads to a G0/G1 phase of cell cycle arrest. Additionally, Ir1Lipo significantly curbed tumour growth in nude mice. The tumour inhibitory rate was 51.2% (5.6 mg/kg). Therefore, liposome as a drug delivery system greatly enhances anticancer activity of Ir1 by a factor of relatively minor side effects. [ABSTRACT FROM AUTHOR]