Perfusion Flow Rate Research Articles

Optimization of Transcardiac Perfusion for More Accurately Evaluating Biodistribution of Large Molecules

The accurate assessment of drug concentrations in biodistribution studies is crucial for evaluating the efficacy and toxicity of compounds in drug development. As the concentration of biologics in plasma can be higher than in tissue due to their potentially low volume of distribution, transcardiac perfusion is commonly employed to reduce the influence of excess drugs in residual blood. However, there is a lack of consistency in the literature on the conditions and methods of perfusion. To enhance blood removal during transcardiac perfusion, sodium nitrite (NaNO2), a vasodilator, has been widely used with concentrations up to 5% in publications. However, we found that such high NaNO2 could disrupt the BBB during perfusion, which should be avoided in experiments. In this study, we examined the impact of various vasodilators on blood–brain barrier integrity and vascular permeability using the ratio of FITC-Dextran to Texas Red-Dextran (FITC/Texas Red). Additionally, we optimized perfusion conditions—including euthanasia method and perfusion flow rate—based on hemoglobin levels and the FITC/Texas Red ratio in tissues. Despite the superiority of NaNO2 in terms of solubility and cost over other vasodilators, we found that 2% NaNO2 disrupted blood–brain barrier integrity, significantly altering the FITC/Texas Red ratio. In contrast, 100 mM NaNO2 did not significantly affect this ratio. Moreover, under Ketamine/Xylazine (Ket/Xyl) anesthesia, which reduced blood clot formation compared to CO2 euthanasia, 100 mM NaNO2 achieved the lowest hemoglobin levels in the brain. Compared to other vasodilators and the PBS control group, 100 mM NaNO2 decreased the tissue/plasma ratio (Kp,t) but not brain/plasma ratio (Kp,b) of hIgG1 and human transferrin. We have developed a method to efficiently evaluate blood–brain barrier integrity during transcardiac perfusion. The combination of Ket/Xyl anesthesia and 100 mM NaNO2 effectively removes residual blood from tissues without significantly affecting blood vessel permeability.

Usefulness of bilateral cerebral regional oxygen saturation measurements in determining selective cerebral perfusion flow rate in a pediatric patient with aortic arch stenosis: a case report

BackgroundWe report a pediatric case where bilateral regional oxygen saturation (rSO2) measurements were useful in determining the selective cerebral perfusion (SCP) flow rate.Case presentationA 9-year-old Japanese boy, 128 cm tall and weighing 25.6 kg, was scheduled for aortic arch reconstruction due to a 90–100 mmHg pressure gradient. Pediatric-sized oximetry sensors were attached to the bilateral forehead area. The rSO2 levels were 70–80% on the right and 80–90% on the left during cardiopulmonary bypass. Immediately following deep hypothermic circulatory arrest with the body temperature cooled to 25 °C, SCP was initiated from the right brachiocephalic artery at 10 mL/kg/min. As the rSO2 decreased steeply to 43–45% on the right and to 32–38% on the left, the SCP flow was increased to 15 mL/kg/min. The right rSO2 increased promptly to 50–60%, but the left rSO2 remained at 30–40%. After the SCP flow was increased to 20 mL/kg/min, bilateral rSO2 levels of 50–60% were obtained, and the SCP flow rate was maintained. The patient was transferred to the ICU postoperatively and extubated on the second postoperative day with no neurological abnormalities.ConclusionsBilateral rSO2 measurements are essential even for a pediatric patient undergoing SCP, despite the limited forehead area.

Validation of advanced hybrid SPECT/CT system using dynamic anthropomorphic cardiac phantom

ObjectiveMyocardial blood flow (MBF) assessment can provide incremental diagnostic and prognostic information and thus the validation of dynamic SPECT is of high importance. We recently developed a novel cardiac phantom for dynamic SPECT validation and compared its performance against the GE Discovery NM 530c. We now report its use for validation of a new hybrid SPECT/CT System featuring advanced cadmium zinc telluride (CZT) technology in a ring array detector design (StarGuide™, GE HealthCare).MethodsOur recently developed cardiac phantom with injected technetium-99m radiotracer was used to create physiological time activity curves (TACs) for the left ventricular (LV) cavity and the myocardium. The TACs allow the calculation of uptake rate (K1) and MBF. The StarGuide system was used to acquire and process the TACs, and these were compared to the TACs produced by the phantom and its mathematical model. Fifteen (15) experiments with different doses representing various MBF values were conducted, and a standard statistic tool was applied for significance.ResultsThe TACs produced by the StarGuide system had a significant correlation (p < 0.001) with the reference TACs generated by the phantom both for the LV (r = 0.94) and for the myocardium (r = 0.89). The calculated MBF difference between the system and the phantom was 0.14 ± 0.16 ml/min/g and the average relative absolute difference was 13.2 ± 8.1%. A coefficient of variance of ≤ 11% was observed for all MBF subranges. The regional uptake rate values were similar to the global one with a maximum difference of 5%.ConclusionsOur newly developed dynamic cardiac phantom was used for validation of the dynamic hybrid SPECT/CT CZT-based system (StarGuide™, GE). The accuracy and precision of the system for assessing MBF values were high. The new StarGuide system can reliably perform dynamic SPECT acquisitions over a wide range of myocardial perfusion flow rates.

Treatment strategies of cytoreductive surgery plus intraperitoneal hyperthermic chemotherapy for gastric cancer with peritoneal metastasis: a systematic review

Peritoneal metastasis in gastric cancer is associated with rapid disease progression. Hyperthermic intraoperative peritoneal chemotherapy (HIPEC) done immediately after cytoreductive surgery (CRS) has become an important treatment for peritoneal metastasis in gastric cancer patients. However, different treatment options for HIPEC exist with potential influence on survival rates and prognosis in patients, exist. These treatment options include open or closed abdomen technique, perfusion solution, number of catheters, temperature, duration, and drug regimens. This paper aims to provide more evidence on standardization of HIPEC treatment options and technologies by systematically reviewing different drug regimens and technical approaches. The study included 2 randomized controlled trials, 3 phase I/II clinical trials, 2 prospective cohort studies, and 34 retrospective cohort studies, involving 1511 patients. The most common HIPEC option is to dissolve 50-75 mg/m2 of Cisplatin and 30-40 mg/m2 of Mitomycin C in 3-4 L saline solution at 42-43℃. After gastrointestinal anastomosis, 2-3 catheters are used in the HIPEC system with a perfusion flow rate of 500 ml/min. The duration is 60-90 minutes. Anastomotic leakage was low in studies where HIPEC was performed after gastrointestinal anastomosis. The utilization of open HIPEC and a two-drug regimen resulted in improved overall survival rates. The future development of HIPEC aims to enhance tumor-specific therapy by optimizing various aspects, such as identifying the safest and most effective chemotherapy regimens, refining patient selection criteria, and improving perioperative care.

An Integrated and Modular Compartmentalized Microfluidic System with Tunable Electrospun Porous Membranes for Epithelialized Organs-on-a-Chip.

A modular and 3D compartmentalized microfluidic system with electrospun porous membranes (PMs) for epithelialized organ-on-a-chip systems is presented. Our novel approach involves direct deposition of polymer nanofibers onto a patterned poly(methyl methacrylate) (PMMA) substrate using electrospinning, resulting in an integrated PM within the microfluidic chip. The in situ deposition of the PM eliminates the need for additional assembly processes. To demonstrate the high throughput membrane integration capability of our approach, we successfully deposited nanofibers onto various chip designs with complex microfluidic planar structures and expanded dimensions. We characterized and tested the fully PMMA chip by growing an epithelial monolayer using the Caco-2 cell line to study drug permeability. A comprehensive analysis of the bulk and surface properties of the membrane's fibers made of PMMA and polystyrene (PS) was conducted to determine the polymer with the best performance for cell culture and drug transport applications. The PMMA-based membrane, with a PMMA/PVP ratio of 5:1, allowed for the fabrication of a uniform membrane structure along the aligned nanofibers. By modulating the fiber diameter and total thickness of the membrane, we could adjust the membrane's porosity for specific cell culture applications. The PMMA-PVP nanofibers exhibited a low polydispersity index value, indicating monodispersed nanofibers and a more homogeneous and uniform fiber network. Both types of membranes demonstrated excellent mechanical integrity under medium perfusion flow rates. However, the PMMA-PVP composition offered a tailored porous structure with modulable porosity based on the fiber diameter and thickness. Our developed platform enables dynamic in vitro modeling of the epithelial barrier and has applications in drug transport and in vitro microphysiological systems.

Cerebral Oxygen Saturation Associates with Changes in Oxygen Transport Parameters during Cardiopulmonary Bypass.

(1) Background: Adequate organ perfusion during cardiopulmonary bypass (CPB) requires accurate estimation and adjustment of flow rates which conventional methods may not always achieve. Perioperative monitoring of cerebral oxygen saturation (ScO2) may detect changes in oxygen transport. This study aims to compare estimated and measured perfusion flow rates and assess the capacity of ScO2 to detect subtle changes in oxygen transport during CPB. (2) Methods: This observational study included 50 patients scheduled for elective coronary artery bypass grafting (CABG) surgery, all of whom provided written informed consent. Perfusion flow rates were estimated using the DuBois formula and measured using echocardiography and a flow probe in the arterial line of the CPB system. ScO2 was continuously monitored, alongside intermittent measurements of oxygen delivery and extraction ratios. (3) Results: Significant discrepancies were found between estimated flow rates (5.2 [4.8-5.5] L/min) and those measured at the start of the surgery (4.6 [4.0-5.0] L/min). These discrepancies were flow rate-dependent, being more pronounced at lower perfusion rates and diminishing as rates increased. Furthermore, ScO2 showed a consistent correlation with both oxygen delivery (r = 0.48) and oxygen extraction ratio (r = 0.45). (4) Conclusions: This study highlights discrepancies between estimated and actual perfusion flow rates during CPB and underscores the value of ScO2 monitoring as a continuous, noninvasive tool for maintaining adequate organ perfusion, suggesting a need for improved, patient-tailored perfusion strategies.

Fluid absorption during flexible ureteroscopy with intelligent control of renal pelvic pressure: a randomized controlled trial.

To investigate fluid absorption and its influencing factors during flexible ureteroscopy with intelligent control of renal pelvic pressure (RPP). A total of 80 patients with upper urinary tract calculi underwent flexible ureteroscopy with intelligent control of RPP by pressure-measuring ureteral access sheath and were randomly divided into four groups. The RPP of Groups A, B, and C were set at -5, 0 and 5mmHg, respectively. Conventional flexible ureteroscopy with uncontrolled pressure served as control Group D. The perfusion flow rate was set at 100ml/min in the four groups, with 20 patients in each group. The fluid absorption was measured by 1% ethanol every 10min. Operation time, stone-free rate, and complications were recorded. Seventy-three patients were finally included in the RCT. The general and preoperative data of the patients were comparable between the groups. The fluid absorption of Groups A, B, and C was significantly less than that of Group D (P < 0.01). Fluid absorption and operation time were positively correlated, and the correlation coefficients R were 0.864, 0.896, 0.918, and 0.947, respectively (P < 0.01). The fluid absorption of patients with vomiting, fever and ureteral injury was greater than that of patients without complications in the four groups (P < 0.01). In different groups, fluid absorption was greater in patients with ureteral injury Post-Ureteroscopic Lesion Scale (PULS) 1-3 than in noninjured patients (P < 0.01). Flexible ureteroscopy with intelligent control of RPP effectively reduces the absorption of perfusion fluid. Operation time and ureteral injury are also key factors affecting perfusion fluid absorption. NCT05201599; August 11, 2021.

Intrarenal pressure detection during flexible ureteroscopy with fiber optic pressure sensor system in porcine model

To validate the feasibility of a fiber-optic pressure sensor-based pressure measurement device for monitoring intrarenal pressure and to analyze the effects of ureteral acess sheath (UAS) type, surgical location, perfusion flow rate, and measurement location on intrarenal pressure (IRP). The measurement deviations and response times to transient pressure changes were compared between a fiber-optic pressure sensing device and a urodynamic device IRP in an in vitro porcine kidney and in a water tank. Finally, pressure measurements were performed in anesthetized female pigs using fiber-optic pressure sensing device with different UAS, different perfusion flow rates, and different surgical positions at different renal calyces and ureteropelvic junctions (UPJ). According to our operation, the result is fiber optic pressure sensing devices are highly accurate and sensitive. Under the same conditions, IRP varied among different renal calyces and UPJ (P < 0.05). IRP was lowest at 50 ml/min and highest at 150 ml/min (P < 0.05). Surgical position had a significant effect on IRP (P < 0.05). 12/14 Fr UAS had a lower IRP than 11/13 Fr UAS. Therefore fiber optic pressure sensing devices are more advantageous for IRP measurements. In ureteroscopy, the type of ureteral sheath, the surgical position, the perfusion flow rate, and the location of the measurement all affect the intrarenal pressure value.

Abstract 6790: Breaking barriers: A high-throughput 3D drug discovery platform for ovarian cancer

Abstract Background: Ovarian Cancer (OVCA) is a formidable challenge in oncology and remains the most lethal gynecologic malignancy with many cases (~80%) diagnosed at a late stage with an equally high rate of recurrence. Yet, no established OVCA models exist that faithfully recapitulate the biological complexity of metastatic OVCA. This multidisciplinary team developed a new in vitro high-throughput model that maintains the characteristics of the patient’s tumor including resident immune cells. Key breakthroughs include long term (&amp;gt;21 day) culture of patient-derived microtumors, a functional and perfusable microgel medium (Liquid Like Solids - LLS™), microplates with controlled “pumpless” perfusion of culture media (Darcy Plates™), and integrated in situ imaging. Methods: We designed, fabricated, and validated a new 3D culture device in the standard SBS microplate format (Darcy Plate) that integrates in situ microscopy and perfusion through a bio-conjugated microgel bed (LLS). Patient tumors were collected during debulking surgery, micronized into 1 µl microtumors, suspended in LLS, and plated into the 48-well Darcy Plate. Viability and proliferation were assessed over 21 days in situ using a standard LIVE/DEAD™ kit and EDU staining, respectively. Epithelial OVCA cells and immune cells were identified with immunofluorescence microscopy. Results: Optimal media conditions (HPLM media with 10% FBS, 1% Pen/Strep, 2.5 mg L−1 Amphotericin B, 10 mM HEPES, 0.5 µM A83-01 -TGF-β inhibitor-, and ITS) and perfusion flow rates (100 µl/day per well) were identified that resulted in outstanding cell viability after 21 days (~100% - no detectable cell death using LIVE/DEAD™). PAX8 nuclear expression, a marker for epithelial metastatic OVCA, was retained. EDU staining confirmed cell proliferation and CD45 staining revealed retention of viable immune cells on and within the microtumor at 21 days. Drug testing to evaluate tumor response to chemotherapeutic agents, carboplatin, and emerging targeted therapies was performed by dosing the feed-wells at different concentrations and evaluating cell death through LIVE/DEAD imaging after 5 days of treatment. Conclusions: OVCA is a challenging disease with understudied biological complexity and extensive metastatic involvement. This study demonstrates that drug screening with 3D microtumors has important clinical implications and provides a unique opportunity to evaluate drug responses and personalized treatment strategies. These patient-derived microtumors retain crosstalk between diverse cell populations and the tumor microenvironment, which increases the likelihood of identifying effective therapies and drug candidates. This system retains patient-specific tumor heterogeneity and microenvironmental complexity of OVCA, offering a promising platform for drug screening, high-throughput assays, biomarker discovery, and ultimately improving treatment outcomes. Citation Format: Erin George, Diego I. Pedro, Alfonso Pepe, Angie M. Rivera, Ryan A. Smolchek, Jack E. Famiglietti, W. Gregory Sawyer. Breaking barriers: A high-throughput 3D drug discovery platform for ovarian cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 6790.

O242: Prolonged subnormothermic acellular machine perfusion of human kidneys

Abstract Introduction Prolonged periods of ex vivo perfusion are required to effectively deliver regenerative therapies directly to a kidney before transplantation. This provides time to start repair processes and reduce the likelihood of early graft dysfunction. The aim of this study was to assess the capability of extending the preservation interval using subnormothermic acelllular machine perfusion (SNAP). Methods After a period of static cold storage, 12 human kidneys declined for transplantation were perfused with an oxygenated human serum albumin-based solution at 32°C for 6, 12 or 24h (n=4 per group). After preservation all kidneys were reperfused with a red blood cell-based solution at 37°C for 4h for assessment. Results Functional parameters remained stable during SNAP in all kidneys. However, the perfusate flow rate was significantly lower in the 24h group (24h 166±45, 12h 266±45, 6h 214±36 mL/min/100g; P=0.008). After reperfusion, levels of urinary neutrophil gelatinase-associated lipocalin (uNGAL), insulin-like growth factor binding protein 7 (IGFBP7) and liver-type fatty acid-binding protein (L-FABP) were similar between groups (P&amp;gt;0.05). Levels of oxygen consumption were significantly lower in 24h kidneys compared to 12h (24h 1.45±0.86, 12h 4.3±1.78 mL/min/100g; P=0.0294). Histological evaluation showed a preserved renal morphology in all kidneys, except for the 24h group which showed a mild increase in tubular and endothelial damage. Conclusion This study demonstrated that human kidneys can be successfully preserved with SNAP for up to 12h. There was some evidence of additional ischaemic injury in the 24h SNAP kidneys which warrants further investigation.

The Number of Microbubbles Generated During Cardiopulmonary Bypass Can Be Estimated Using Machine Learning From Suction Flow Rate, Venous Reservoir Level, Perfusion Flow Rate, Hematocrit Level, and Blood Temperature.

Microbubbles (MBs) are known to occur within the circuits of cardiopulmonary bypass (CPB) systems, and higher-order dysfunction after cardiac surgery may be caused by MBs as well as atheroma dispersal associated with cannula insertion. As complete MB elimination is not possible, monitoring MB count rates is critical. We propose an online detection system with a neural network-based model to estimate MB count rate using five parameters: suction flow rate, venous reservoir level, perfusion flow rate, hematocrit level, and blood temperature. Perfusion experiments were performed using an actual CPB circuit, and MB count rates were measured using the five varying parameters. Bland-Altman analysis indicated a high estimation accuracy (R2 > 0.95, p < 0.001) with no significant systematic error. In clinical practice, although the inclusion of clinical procedures slightly decreased the estimation accuracy, a high coefficient of determination for 30 clinical cases (R2 = 0.8576) was achieved between measured and estimated MB count rates. Our results highlight the potential of this system to improve patient outcomes and reduce MB-associated complication risk.

Research on dynamic perfusion control technology of 3D printed tissue vascular network

In order to solve the problem that the medium cannot be supplied accurately during the perfusion culture of the vascular network in large-volume 3D printing tissue, a perfusion control technology was studied by designing and building an in vitro perfusion and monitoring platform with feedback regulation. First, a large-volume vascular network of hydrogel material was fabricated by 3D bioprinting technology as the experimental object of perfusion. Then we designed and built the dynamic perfusion device and the monitoring equipment in the perfusion process independently and applied the real-time flow calibration control technology on this basis. Finally, the accuracy of the flow real-time calibration control technology was verified through the perfusion experiment of the large-volume vascular network. The results showed that the error rate between the actual flow rate and the preset flow rate increased gradually with the decrease of the preset flow rate of medium perfusion. When the preset flow is 3 mL/min, the error rate between them is as high as 19.33% without the application of flow calibration control technology. The dynamic perfusion device can reduce the average error rate between the two from 8.1% to 0.4% after applying real-time flow calibration control technology, which proves that the device can cultivate a large-volume vascular network with high-precision perfusion after the application of real-time flow calibration control technology.

Study on Microfluidic Chip Flow Rate Uniformity for Cell Activity Detection.

During the cell viability detection process inside a microfluidic chip, the more uniform the distribution of medium flow rates, the higher the accuracy of detection results. In order to achieve this goal, a multichannel microfluidic chip with uniform distribution of medium flow rates has been successfully designed. The multichannel microfluidic chip is designed with cell injection channels, vascular network-shaped medium injection channels, buffer zones, and a culture chamber. The medium flow rates inside culture chambers of the multichannel microfluidic chip and the common single-channel microfluidic chip are compared by COMSOL Multiphysics software and particle velocimetry experiment. The simulation and experimental results show that the medium flow rate distribution inside the culture chamber of the multichannel microfluidic chip is more uniform and changes more smoothly. When the medium perfusion flow rate is 0.5 μL/min, the maximum flow rate difference inside the culture chamber of the single-channel microfluidic chip is more than 13 times that of the multichannel microfluidic chip. Therefore, the multichannel microfluidic chip can ensure a uniform supply of medium inside the culture chamber, which is beneficial to improve the accuracy of cell viability detection.

Development of a Novel Ex Vivo Porcine Hepatic Segmental Perfusion Proof-of-Concept Model Towards More Ethical Translational Research.

Introduction Ex vivo machine perfusion describes the technique where organs are continuously perfused and oxygenated extracorporeally (at physiological conditions) to maintain the organs' viability. To our knowledge, there are currently no reported studies describing ex vivo perfusion of a single hepatic segment. Here, we describe the development of a porcine ex vivo hepatic segmental perfusion model to demonstrate proof of concept and support further research into the ex vivo perfusion of the human liver using discarded tissue. Methods Whole livers were retrieved from abattoir-derived pigs and connected to a normothermic extracorporeal perfusion circuit. Constant segmental perfusion via the common or segmental hepatic artery and portal vein with heparinised autologous blood was established. The viability of the perfused organ was assessed by monitoring perfusion pressures, flow rates and histology samples. Results Following perfusion and optimisation of the model for three hepatic segments, the third perfusion demonstrated viable hepatocytes centrally after 4 hof segmental perfusion. Conclusion Ex vivo hepatic segmental perfusion is technically challenging but its success in a porcine model and the principles learned should facilitate the development of an analogous human model using discarded tissue following formal liver resections. The model would usea healthy liver segment following a major formal resection such as a hemi-hepatectomy and ex vivo perfusion performed via a segmental hepatic artery and portal vein. If successful this model would represent a significant development and enableethical translation research to assess the response of human livers to a variety of stressors, including toxicity and infection.

Extensive Peritonectomy is an Independent Risk Factor for Cisplatin HIPEC-Induced Acute Kidney Injury

BackgroundCisplatin (CDDP)-containing hyperthermic intraperitoneal chemotherapy (HIPEC) is frequently applied in selected patients with peritoneal malignancies derived from ovarian cancer, gastric cancer, and primary peritoneal mesothelioma. HIPEC with CDDP increases perioperative morbidity, in particular by inducing acute kidney injury (AKI). Factors contributing to occurrence of AKI after intraperitoneal perfusion with CDDP have not been sufficiently evaluated.Patients and MethodsData from 63 patients treated with a CDDP-containing HIPEC regimen were retrospectively analyzed concerning demographics, underlying disease, surgery, and HIPEC details to evaluate risk factors of AKI. A preclinical rat perfusion model was applied to assess the influence of temperature, concentration, perfusate volume, perfusion flow rate, and extent of peritonectomy on drug absorption upon intraperitoneal CDDP perfusion.ResultsAKI occurred in 66.1% of patients undergoing CDDP-containing HIPEC, with total intraoperative fluid influx being a negative and the extent of parietal peritonectomy being a positive independent predictor of postoperative AKI. In a preclinical model, bilateral anterior parietal peritonectomy significantly increased systemic CDDP absorption by 1.6 to 2-fold. CDDP plasma levels in animals were significantly higher after both perfusion with increased CDDP perfusate concentrations and bilateral anterior parietal peritonectomy.ConclusionCDDP-containing HIPEC is associated with relevant morbidity owing to its systemic toxicity. Extent of parietal peritonectomy is an independent predictor of AKI. CDDP dose reduction should be considered in case of extensive parietal peritonectomy. Cytostatic drug concentrations in HIPEC perfusate should be paid more attention to than total dose per body surface area. Further clinical studies are needed to confirm the presented preclinical findings.

Pharmacokinetics of three index components of Periploca forrestii in rats by microdialysis combined with UPLC-MS/MS

The present study established a UPLC-MS/MS method for the content determination of Periploca forrestii microdialysis samples and investigated the pharmacokinetics of three index components of P. forrestii in rats. The effects of flow rate and concentration of perfusate on the recovery rate were investigated by the concentration difference method(increment method and decrement method). The microdialysis samples at different time points were collected, and the concentrations of three index components were determined by UPLC-MS/MS. The actual drug concentrations were corrected with the in vivo recovery rate, and the pharmacokinetic parameters were calculated by WinNonlin 8.2. In the in vitro recovery test, the recovery rate measured by the increment method and the decrement method was inversely proportional to the flow rate and independent of the concentration. The pharmacokinetic parameter AUC_(0-t) values of 3-O-caffeoyl quinic acid, 4-O-caffeoyl quinic acid, and 5-O-caffeoyl quinic acid were(23 911.23±5 679.67),(16 688.43±3 448.45), and(9 677.02±1 606.74) min·μg·L~(-1), respectively. C_(max) values were(170.66±58.02),(121.61±48.14), and(69.69±18.23) μg·L~(-1), respectively. The UPLC-MS/MS method has the advantages of specificity, rapidity, high sensitivity, and accurate quantification. It can simultaneously determine the concentration of 3-O-caffeoyl quinic acid and other two index components in microdialysis samples and is suitable for the pharmacokinetics study of the three index components of P. forrestii in normal rats.

Effect of Co-culture of mesenchymal stem cell and glomerulus endothelial cell to promote endothelialization under optimized perfusion flow rate in whole renal ECM scaffold.

In recent era, many researches on implantable bio-artificial organs has been increased owing to large gap between donors and receivers. Comprehensive organ based researches on perfusion culture for cell injury using different flow rate have not been conducted at the cellular level. The present study investigated the co-culture of rat glomerulus endothelial cell (rGEC) and rat bone marrow mesenchymal stem cells (rBMSC) to develop micro vascularization in the kidney scaffolds culturing by bioreactor system. To obtain kidney scaffold, extracted rat kidneys were decellularized by 1% sodium dodecyl sulfate (SDS), 1% triton X-100, and distilled water. Expanded rGECs were injected through decellularized kidney scaffold artery and cultured using bioreactor system. Vascular endothelial cells adhered and proliferated on the renal ECM scaffold in the bioreactor system for 3, 7 and 14 days. Static, 1​ml/min and 2​ml/min flow rates (FR) were tested and among them, 1​ml/min flow rate was selected based on cell viability, glomerulus character, inflammation/endothelialization proteins expression level. However, the flow injury was still existed on primary cell cultured at vessel in kidney scaffold. Therefore, co-culture of rGEC​+​rBMSC found suitable to possibly solve this problem and resulted increased cell proliferation and micro-vascularization in the glomerulus, reducing inflammation and cell death which induced by flow injury. The optimized perfusion rate under rGEC​+​rBMSC co-culture conditions resulted in enhanced endocellularization to make ECM derived implantable renal scaffold and might be useful as a way of treatment of the acute renal failure.

Applicability of the microdialysis technique in dry soils: Impact of soil water content depends on perfusion flow rate

Plant nutrient acquisition largely depends on the availability and constant replenishment of nutrients at root surfaces. The main process providing nutrients for root uptake is diffusion which is critically affected by soil physicochemical and biological factors. The effective diffusion path length increases with decreasing soil water content thus limiting diffusive nutrient supply in dry soils. Microdialysis, an increasingly popular sampling tool for monitoring nutrient fluxes in soil in situ, could be used to measure such a limitation provided it operates reliably under dry soil conditions. However, due to its mode of operation, the performance of microdialysis could be impeded in dry soils since a significant amount of perfusate might be lost via leaching to the surrounding soil. Until now, however, no data is available on the applicability of microdialysis in dry soils. In this project, we estimated leaching losses of perfusate to eight soils with different texture maintained at 10, 20, 30, 50 and 80% (w/w) of maximum water-holding capacity in dependence of perfusion flow rate. We found that microdialysis operates reliably even in dry soils when using a high perfusion flow rate (10 μl min−1). At lower perfusion flow rates (1 or 5 μl min−1), however, significant amounts of perfusate were leaching out to soils. Diffusive fluxes of nitrate and ammonium were strongly affected by soil water content, but not fluxes of phosphate. Even at the highest flow rate (where no losses of perfusate where observed) concentrations of both inorganic N forms in dialysates decreased with decreasing soil water content. Overall, we conclude that microdialysis can be applied in dry soils without high risk of perfusate leaching when a high perfusion flow rate (10 μl min−1) is used. Further, our results highlight that microdialysis can be used in much dryer soils than previously suggested (70% MWHC) and allows monitoring the effect of soil water content on nutrient supply for root uptake via diffusion.

Parametric study of a microdialysis probe and study of depletion effect using ethanol as a test analyte

Although microdialysis is a common in vivo sampling technique, a detailed characterization of the performance of a microdialysis probe used for sampling ethanol molecules has not been conducted. In this work, experimental and computational investigations were carried out to quantitatively study ethanol diffusion characteristics for home-made and commercially available probes. Probe efficiency, i.e. recovery rate (defined as the ethanol concentration in the dialysate to that in the external medium surrounding the probe) was used to characterize the performance. The recovery rate was measured at different perfusion flow rates (0.1, 0.2, 0.5, 1, 1.5, 2 μL/min) and external ethanol concentrations (1, 2.5, 5, 10, 20 mM) with controlled environmental conditions. Effect of temperature was also investigated at 19, 37 and 47 °C. The results show that reducing the flow rate from 2 to 0.1 μL/min at least triples the recovery rate for the home-made probes, and it remains nearly unchanged when varying external ethanol concentration. The performance for two commercial microdialysis probes with different membrane materials and configurations were also determined and have similar recovery rates. Through computational modeling, the diffusion coefficient of ethanol in the semipermeable membrane of the home-made probe was determined by fitting the experimental data, and it was found to be 9 × 1011 m2/s (R2 > 0.99). In addition, the depletion effect over time at different flow rates along with estimated in vivo ethanol clearance were simulated numerically, showing that the depletion region shrinks significantly when the flow rate is below 1 μL/min. The results provide better understanding of the diffusion characteristics of the microdialysis probe when used for sampling ethanol which can be used for better interpretation of in vivo measurements and for microdialysis probe optimization.

Monitoring, Control System Development, and Experimental Validation for a Novel Extrapulmonary Respiratory Support Setup

This article presents a novel mechatronic setup intended for providing respiratory support to patients suffering from pulmonary failure. The setup relies upon the circulation of an oxygenated perfluorocarbon (PFC) through the abdominal cavity. Such circulation provides a potential pathway for the transport of oxygen to the bloodstream. However, the viability of this technology for <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$\text{CO}_2$</tex-math></inline-formula> clearance has not been established. Moreover, there is a lack of experimental data enabling the modeling and identification of the underlying dynamics of this technology. To address these gaps, we develop a flexible experimental perfusion setup capable of monitoring and controlling key variables, such as perfusate flowrate, temperature, pressure, and oxygenation. One important scientific objective of this setup is to enable the measurement of the impact of abdominal PFC perfusion on <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$\text{CO}_2$</tex-math></inline-formula> clearance. The article 1) summarizes the design of this setup; 2) highlights the degree to which its data acquisition system enables the collection and cross-correlation of both perfusion-related and physiological variables; and 3) discusses the development of flow, pressure, and temperature control algorithms for the setup. Experiments with large animals (swine) show that perfusion can potentially affect both <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$\text{O}_2$</tex-math></inline-formula> and <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$\text{CO}_2$</tex-math></inline-formula> dynamics, and that the setup succeeds in recording key data needed for modeling these dynamics.