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2.
Eur J Surg Oncol ; 47(6): 1434-1440, 2021 06.
Article in English | MEDLINE | ID: mdl-33637371

ABSTRACT

BACKGROUND: Icodextrin (IDX) is an antiadhesive polymer that can be used as a carrier solution for intraperitoneal (IP) delivery of chemotherapeutic drugs. METHODS: We investigated the suitability of IDX solution as a carrier of Cisplatin and Doxorubicin for delivery as pressurized intraperitoneal aerosol chemotherapy (PIPAC). We examined the sprayability of IDX, the aerosol characteristics, the stability of the molecule after aerosolization, the effects of IDX on the adhesion of MKN45 human gastric cancer cells, the synergistic effect of aerosolized IDX with Cisplatin and Doxorubicin, and the chemical stability of IDX, Cisplatin, and Doxorubicin in combination. RESULTS: Delivery of IDX as PIPAC is feasible with no particular restrictions. The median droplet size of 35.7 µm did not change at increasing concentrations. IDX withstood the shear forces applied by the nebulizer and remained stable after aerosolization (ANOVA, p = 0.97). IDX did not impair the cytotoxic effects of Cisplatin and Doxorubicin (ns). IDX had a significant antiadhesive impact alone (p < 0.03) and in combination with Cisplatin and Doxorubicin (p < 0.02). IDX as a carrier for Cisplatin and Doxorubicin remained stable at 4 °C for three months and did not cause degradation of those two substances. CONCLUSION: The proposed combination takes advantage of the antiadhesive properties of IDX, the cytotoxic effect of Cisplatin and Doxorubicin, and an advanced drug delivery system.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Cell Adhesion/drug effects , Cell Proliferation/drug effects , Dialysis Solutions/administration & dosage , Icodextrin/administration & dosage , Aerosols , Antineoplastic Combined Chemotherapy Protocols/chemistry , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Cell Line, Tumor , Cisplatin/administration & dosage , Cisplatin/chemistry , Dialysis Solutions/chemistry , Doxorubicin/administration & dosage , Doxorubicin/chemistry , Drug Stability , Humans , Icodextrin/chemistry , Icodextrin/pharmacology , Peritoneum , Pressure
3.
J Surg Res ; 234: 325-333, 2019 02.
Article in English | MEDLINE | ID: mdl-30527492

ABSTRACT

BACKGROUND: The use of surgical meshes in ventral hernia repair has significantly reduced hernia recurrence rates. However, when placed intraperitoneally prosthetic materials can trigger the development of peritoneal adhesions. The present experimental study evaluated the combined icodextrin 4% and dimetindene maleate treatment in preventing peritoneal adhesion formation to polypropylene and titanium-coated polypropylene meshes. MATERIALS AND METHODS: Sixty female white rabbits were divided into four groups. A 2 × 2 cm piece of mesh was fixed to intact peritoneum in all animals through a midline laparotomy. A lightweight polypropylene mesh was implanted in groups 1 and 2 and a titanium-coated polypropylene mesh in groups 3 and 4. Groups 2 and 4 were treated, intraoperatively, with intravenous dimetindene maleate (0.1 mg/kg) and intraperitoneal solution of icodextrin 4% (20 mL/kg) and for the next 6 d with dimetindene maleate intramuscularly. The observation period lasted 15 d. Adhesion scores, percentage of mesh affected surface, tissue hydroxyproline levels, and tissue histopathology were examined. RESULTS: All animals in group 1 and 57% of animals in group 3 presented postoperative adhesions. The combination of antiadhesives significantly reduced the extent and severity of adhesions as well as the hydroxyproline levels in groups 2 and 4 compared with groups 1 and 3. On microscopic evaluation, animals in group 1 exhibited higher inflammation scores compared with group 2, whereas animals in groups 2 and 4 had better mesotheliazation compared with groups 1 and 3. CONCLUSIONS: The combined administration of icodextrin 4% and dimetindene maleate reduces the extent and severity of adhesions and may be successfully used to prevent adhesion formation after mesh intraperitoneal placement.


Subject(s)
Dimethindene/administration & dosage , Icodextrin/administration & dosage , Polypropylenes/adverse effects , Postoperative Complications/prevention & control , Protective Agents/administration & dosage , Surgical Mesh/adverse effects , Tissue Adhesions/prevention & control , Animals , Dimethindene/therapeutic use , Drug Therapy, Combination , Female , Icodextrin/therapeutic use , Injections, Intramuscular , Injections, Intraperitoneal , Injections, Intravenous , Postoperative Complications/etiology , Protective Agents/therapeutic use , Rabbits , Random Allocation , Treatment Outcome
4.
BMC Nephrol ; 19(1): 109, 2018 05 08.
Article in English | MEDLINE | ID: mdl-29739354

ABSTRACT

BACKGROUND: This study aimed to evaluate the longitudinal changes in cardiac structure and function in incident-automated peritoneal dialysis (APD) patients. METHODS: We conducted a 2-year prospective, randomized, open-label, parallel-group study to compare the efficacy of icodextrin solution versus glucose-based solution. Echocardiography was performed at baseline, 1 and 2 years. Echocardiographic parameters over 2 years were evaluated for each group, using the Friedman test. Generalized linear regression analysis was used to test the associations between baseline clinical variables and echocardiographic changes, and a multivariate model was used to analyze cardiac function between the two groups. RESULTS: A total of 43 APD patients were enrolled in the beginning of this study. Twenty patients in the icodextrin group (ICO) and 18 patients in the glucose group (GLU) completed the study. In left ventricular (LV) systolic function measurements, ejection fraction (EF) increased significantly in the GLU group. Measurements of LV diastolic function and septal early mitral annulus velocity (EMV) increased significantly from baseline to 24-months in the ICO group (5.43-5.51 ms). The GLU group showed a significant decrease in peak early diastolic velocity (EDV) (70.67-68.25 cm/s), but a significant increase in septal EMV (5.94-7.57 ms) from baseline to 24-months. No significant association was found between the baseline clinical variables and echocardiographic changes within 24 months in the generalized linear regression analysis. Multivariate models were used to investigate changes in the four primary endpoints, namely, myocardial performance index (MPI), left ventricular ejection fraction (LVEF), deceleration time (DT), and E/e' ratio. These primary endpoints show no significant association with the baseline values in both the ICO and GLU groups. CONCLUSION: The present study demonstrates that long-dwell icodextrin solution can maintain reasonable cardiac structure and function in incident-APD patients. TRIAL REGISTRATION: ISRCTN14931270 (retrospectively registered on 23/03/2018).


Subject(s)
Dialysis Solutions/administration & dosage , Glucose/administration & dosage , Heart/diagnostic imaging , Icodextrin/administration & dosage , Peritoneal Dialysis/trends , Female , Heart/drug effects , Heart/physiology , Heart Diseases/diagnostic imaging , Heart Diseases/therapy , Humans , Incidence , Kidney Diseases/diagnostic imaging , Kidney Diseases/therapy , Longitudinal Studies , Male , Peritoneal Dialysis/adverse effects , Prospective Studies , Ventricular Function, Left/drug effects , Ventricular Function, Left/physiology
5.
Basic Clin Pharmacol Toxicol ; 123(4): 494-503, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29753311

ABSTRACT

Metabolic syndrome (MetS) is commonly observed among peritoneal dialysis (PD) patients, and hyperbranched polyglycerol (HPG) is a promising glucose-sparing osmotic agent for PD. However, the biocompatibility of a HPG-based PD solution (HPG) in subjects with MetS has not been investigated. This study compared the local and systemic effects of a HPG solution with conventional physioneal (PYS) and icodextrin (ICO) PD solutions in rats with MetS. Obese type 2 diabetic ZSF1 rats received a daily intraperitoneal injection of PD solutions (10 mL) for 3 months. The peritoneal membrane (PM) function was determined by ultrafiltration (UF), and the systemic responses were determined by profiling blood metabolic substances, cytokines and oxidative status. Tissue damage was assessed by histology. At the end of the 3-month treatment with PD solutions, PM damage and UF loss in both the PYS and ICO groups were greater than those in the HPG group. Blood analyses showed that compared to the baseline control, the rats in the HPG group exhibited a significant decrease only in serum albumin and IL-6 and a minor glomerular injury, whereas in both the PYS and ICO groups, there were more significant decreases in serum albumin, antioxidant activity, IL-6, KC/GRO (CXCL1) and TNF-α (in ICO only) as well as a more substantial glomerular injury compared to the HPG group. Furthermore, PYS increased serum creatinine, serum glucose and urine production. In conclusion, compared to PYS or ICO solutions, the HPG solution had less adverse effects locally on the PM and systemically on distant organs (e.g. kidneys) and the plasma oxidative status in rats with MetS.


Subject(s)
Diabetes Mellitus, Type 2/metabolism , Dialysis Solutions/toxicity , Glycerol/toxicity , Icodextrin/toxicity , Kidney/drug effects , Obesity/metabolism , Peritoneal Dialysis/adverse effects , Peritoneum/drug effects , Polymers/toxicity , Animals , Biomarkers/blood , Cytokines/blood , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/genetics , Diabetes Mellitus, Type 2/physiopathology , Dialysis Solutions/administration & dosage , Disease Models, Animal , Glycerol/administration & dosage , Icodextrin/administration & dosage , Inflammation Mediators/blood , Injections, Intraperitoneal , Kidney/metabolism , Kidney/physiopathology , Male , Obesity/blood , Obesity/genetics , Obesity/physiopathology , Organic Chemicals/administration & dosage , Organic Chemicals/toxicity , Oxidative Stress/drug effects , Peritoneal Dialysis/methods , Peritoneum/metabolism , Peritoneum/physiopathology , Permeability , Polymers/administration & dosage , Rats, Zucker , Time Factors
6.
Pharmacoepidemiol Drug Saf ; 27(4): 447-452, 2018 04.
Article in English | MEDLINE | ID: mdl-29490427

ABSTRACT

PURPOSE: Icodextrin can enhance ultrafiltration and consequently improve fluid balance and can control blood pressure and reduce left ventricular mass for peritoneal dialysis (PD) patients. This study investigated whether icodextrin use could reduce the risk of congestive heart failure (CHF) for PD patients. METHODS: From the Taiwan National Health Insurance database, we identified 5462 newly diagnosed end-stage renal disease patients undergoing PD from 2005 to 2010. Incidence rates and hazard ratio of CHF were estimated for patients with and without icodextrin treatment by the end of 2011. RESULTS: Among PD patients, icodextrin users had an overall 26% lower incidence of CHF than non-users (13.7 vs 18.6 per 1000 person-years). Relatively, the adjusted hazard ratio was 0.67 (95% CI = 0.52-0.87) for users compared with non-users. Among PD patients with diabetes, the incident CHF in icodextrin users was 37.5% lower than that in non-users (17.8 vs 28.5 per 1000 person-years). Among PD patients without diabetes, the incident CHF in icodextrin users was 30.4% lower than that in non-users (11.0 vs 15.8 per 1000 person-years). CONCLUSIONS: Icodextrin solution could reduce the risk of new-onset CHF, particularly effective when diabetic PD patients use it.


Subject(s)
Dialysis Solutions/administration & dosage , Heart Failure/prevention & control , Icodextrin/administration & dosage , Kidney Failure, Chronic/therapy , Peritoneal Dialysis/methods , Aged , Blood Pressure/drug effects , Comorbidity , Diabetes Mellitus/epidemiology , Female , Heart Failure/epidemiology , Heart Failure/etiology , Heart Ventricles/drug effects , Humans , Incidence , Kidney Failure, Chronic/complications , Kidney Failure, Chronic/epidemiology , Male , Middle Aged , Peritoneal Dialysis/adverse effects , Proportional Hazards Models , Taiwan/epidemiology , Water-Electrolyte Balance/drug effects
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