Journal of Medical Microbiology and Diagnosis-Biotechnology Open Access Journals

Improved Albumin-Derived Per Fluorocarbon- Based Artificial Oxygen Carriers: In-vivo Evaluation of Biocompatibility

Anna Wrobeln, Michael Kirsch and Katja Bettina Ferenz*

Institute of Inorganic Chemistry, University of Duisburg-Essen, Germany

Submission: August 29, 2017; Published: November 27, 2017

*Corresponding author: Katja Bettina Ferenz, Institute for Physiological Chemistry, University of Duisburg- Essen, University Hospital Essen Hufelandstr, 55, 45122 Essen, Germany, Tel: +49-201-723-4106; Fax: +49 201-723-5943; Email: katja.ferenz@uk-essen.de

How to cite this article: Anna W, Michael K, Katja B F. Improved Albumin-Derived Per Fluorocarbon-Based Artificial Oxygen Carriers: In-vivo Evaluation of Biocompatibility. Adv Biotech & Micro. 2017; 7(3): 555714. DOI: 10.19080/AIBM.2017.07.555714

Abstract

Despite long lasting efforts, an artificial oxygen carrier displaying adequate gas solubility combined with a minimal risk of side effects is missing at present for clinical use, both in Europe and USA. To bypass this bottleneck, recently developed albumin-derived per fluorocarbon- based nanocapsules were further improved and tested in-vivo. Most importantly, this second nanocapsule generation reached a smaller size distribution that resulted in partially less side effects compared to the first capsule formulation. The intravenous administration to healthy rats was tolerated without any noticeable abnormalities. Systemic and blood parameters stayed within the physiological range. Minor side-effects could be observed in the release of intracellular enzymes specific for organ damage. The intravascular half -life of the second generation of albumin-derived per fluorocarbon-based nanocapsules was ameliorated with regard to the first generation. Thus, the further improved albumin- derived per fluorocarbon-based nanocapsules should be tested in much more advanced and clinical relevant models

Keywords: Per fluorocarbon-based oxygen carriers; Artificial oxygen carrier; Blood substitutes; Albumin; Nanocapsules; Nano particles; Per fluorocarbon; Perfluorodecalin; Intravenous administration

Abbreviations: ALAT: Alanine Aminotransferase; ASAT: Aspartame Aminotransferase; CK: Creatine Kinase; 19F-NMR: 19F-Nuclear Magnetic Resonance Spectroscopy; HAS: Human Serum Albumin; LDH: Lactate Dehydrogenase; MAP: Mean Arterial Blood Pressure; PFC: Per Fluorocarbon; PFD: Perfluorodecalin; pO₂: Oxygen Dioxide Partial Pressure; pCO₂: Carbon Dioxide Partial Pressure; RI: Refractive Index; VIS: Viscosity

Introduction

The interest in an artificial oxygen carrier as red blood cell replacement continuously increased during the last decades [13]. At the moment the necessity of blood transfusions is growing while the willingness. To donate blood is declining [4-6]. Major requirements for an artificial oxygen carrier are of course the ability to transport both, oxygen and carbon dioxide, but also the possibility to be stored easily for a long time without any loss in quality. Furthermore, the use should not be limited by any blood group characteristics and the oxygen carrier should be present in the blood circulation for a long time, i.e. some hours [7]. One way to overcome these challenges is the use of per fluorocarbons as an artificial oxygen carrier [8-11]. We developed a kind of nanocapsule to encapsulate the blood-incompatible, oxygen- dissolving perfluorodecalin (PFD). For that purpose, we used human serum albumin (HSA) as a membrane around the PFD core. In our previous studies, we characterized the nanocapsules, examined their functionality and performed first in-vivo biocompatibility tests [12,13]. The tests pointed out that the nanocapsules transport physiological relevant amounts of oxygen [12] and are able to supply hypoxic tissues [13]. The previously used nanocapsules showed slight side effects and a too short circulatory in-vivo half-life (158min) which we tried to eliminate by improving the size of the nanocapsules. In this short communication, the performance of the improved nanocapsules will be presented and compared to the first generation.

Materials and Methods

Materials

5% human serum albumin solution (HSA 5%, containing 5% human serum albumin, 0.75% NaCl, 0.11% sodium-N- acetyltryptophanoate, 0.07% sodium caprylate) was purchased from Baxter

(Unterschleissheim, Germany). Perfluorodecalin (PFD) was from Fluorochem Chemicals (Derbyshire, UK).

Methods

Synthesis of capsules: The synthesis of capsules was based on a previously described method [12] with some modifications. Here, 2.5ml of HSA 5% and 0.5ml PFD were combined in a reaction tube with a total capacity of 15ml. The reaction tube was cooled in an ice bath and the mixture was solicited for 10min using a sonotrode with a tip diameter of 3mm associated with a UP 400S ultrasonic processor (Hielscher, Teltow, Germany). For sonication, the tip of the sonotrode was placed at the PFD- water interface. At a power of 400W, ultrasonic amplitudes with 210mm and a frequency of 24kHz were generated.

Determination the capsule diameter: For the determination of the capsule diameter ten different batches of capsules were synthesized. Measurements were performed with a Zetasizer ZS (Malvern Instruments, Zetasizer software Version 7.11.) in intensity mode, with a 173 °C angle (non- invasive backscattering) in a clear disposable zeta cell (Malvern DTS1070) at 25 °C. For the measurement, 50μl of the capsules were diluted in 950μl of the storage media. The refractive index (RI) of the capsule wall material albumin was 1.89 with absorption of 0.01. The parameters (RI and viscosity (Vis)) of the media HSA 5% (outer phase) were as follows: RI = 1.345, Vis 1.25mPa s.

Biocompatibility test animals: As described in our previous study [12] 12 rats were anesthetized with isoflurane (2.0% in 100% medical O₂ at 4.0l/min for induction, 1.5-2.0% isoflurane in 100% medical O₂ at 1.0lmin throughout the experiment) through face masks connected to a vaporizer (Isofluran Vet Med Vapour, Draeger, Luebeck, Germany). For analgesia they received ketamine subcutaneously (50mg/kg body weight) into the right chest wall. After local lidocaine administration (5mg/kg body weight subcutaneously) a median skin-deep inguinal incision of about 2cm was made along the right groin and a Portex catheter (0.58mm ID, 0.96mm OD) was placed within the right femoral artery and the right femoral vein. Each catheter was fixed with a surgical suture. At the end of experiment, animals were sacrificed by resection of the heart under deep isoflurane anesthesia.

Biomonitoring: The mean arterial pressure (MAP) was recorded continuously via the femoral artery catheter. The catheter was connected to a pressure transducer and blood pressure was displayed on a monitor. Heart rates were determined from systolic blood pressure spikes and breathing rates were calculated by counting the ventilation movements per minute every 10min. The body core temperature of the rats was continuously monitored using a rectal sensor. A cooling below 37 °C was prevented by an underlying thermostat-controlled operating table as well as by covering the animals with wrapping film.

Assessment of blood and plasma parameters: Blood samples (0.5ml) for blood gas analysis as well as for the monitoring of enzyme activities in plasma were taken from the femoral artery catheter directly after catheterization of femoralis A, 3min before initiation of infusion and subsequently 30, 60, 90, 120, 150 and 180min after start of the infusion using a 2ml syringe containing 80 IU electrolyte-balanced heparin (Pico50, Radiometer Medical, Brønshøj, Denmark). For each blood sampling, animals were substituted with a 0.5ml bolus of 0.9% NaCl solution via the femoral artery (with the additional effect to keep the catheter functional). In order to obtain plasma, blood was centrifuged at 4500x g for 10min at room temperature. The gained plasma was used straight away for the determination of the activity of released enzymes.

Blood gas analysis: Arterial blood pH, oxygen and carbon dioxide partial pressures (pO₂, pCO₂), base excess, glucose and lactate were assessed with a blood gas analyzer (ABL 715, Radiometer, Copenhagen, Denmark).

Enzyme activities: The plasma activity of lactate dehydrogenase (LDH) as a general marker of cell injury, creatine kinase (CK) as a marker for muscle cell injury, aspartate aminotransferase (ASAT) and alanine aminotransferase (ALAT) as markers for hepatocyte injury were determined using a fully automated clinical chemistry analyzer (Vitalab Selectra E, VWR International, Darmstadt, Germany) using commercially available reagent kits (DiaSys, Holzheim, Germany).

Determination of the circulatory in-vivo half-life: After administration of improved nanocapsules (20ml/kg body weight x h) blood samples were taken from the femoral artery directly at the end of infusion and subsequently 60, 120 and 180 min after the end of infusion. Samples were stored at -80 °C until further analysis by 19F-nuclear magnetic resonance spectroscopy (19F-NMR) and the total amount of PFD within the samples was calculated as described previously [14]. The study group consisted of 3 animals. We assumed a virtual IV bolus model and assumed the intravascular capsule concentration at the time point 30min= tmax to be cmax.

Statistics: Data are expressed as mean values ±SEM for in- vivo experiments. Comparisons among multiple groups were performed using two-way analysis of variance (ANOVA) for repeated measurements followed by Dunnett post hoc analysis. A p-value <0.05 was considered to indicate significance. The groups in Figure 1-3 represent n=6 animals. The analysis of the circulatory in-vivo half-life (Figure 4) was performed with 3 animals per group. The calculation was done by exponential one- phase decay least squares ordinary fit based on the following equation:

Y= (Y0-plateau) x exp (-K x X) + plateau

The half-life was calculated with ln [2]/K. For every statistical analysis, graph pad prism 6.05 (Graph Pad Software Inc, La Jolla, CA, USA) was used.

Result

The capsule diameter

The improvement of the synthesis created nanocapsules with a mean size of about 252nm. The smallest capsules showed a hydrodynamic diameter of 70nm and the biggest ones 692nm, respectively.

Biocompatibility

The biocompatibility results of the first generation nanocapsules are reference data from our previous studies [12]. The improved nanocapsules correspond to the volume- concentration of the first generation nanocapsules (32 Vol %). The mapped controls were done within this work.

Systemic parameters

During the first 30min of the experiment the MAP of the groups remained between 88mmHg and 101 mmHg (Figure 1A). In the control group (HSA 5%) the MAP raised immediately from 98mmHg to 102mmHg within the first 10min of infusion. At the same time the animals of the improved nanocapsules group showed immediately a MAP decline from 101mmHg to 84mmHg. After that the MAP remained stable between 88mmHg and 98mmHg until the end of the experiment. Before infusion, the heart rate (Figure 1B) was found between 264 and 284 beats/ minute in both groups. After the infusion animals of the improved nanocapsules group showed a partly higher heart rate of about 325 beats/minute, compared to the control animals (about 310 beats/minute). In the control group the respiratory frequency (Figure 1C) raised from 51 breaths/minute (immediately before the infusion) up to 57 breaths/minute within 10min of infusion. The animals of the improved nanocapsules group showed a lower respiratory frequency of 45 breaths/minute under similar experimental conditions. Interestingly the respiratory frequency of the animals receiving the second generation nanocapsules (improved ones) raised up to 57 breaths/minute after an infusion period of 30min. After that the respiratory frequency remained stable in both groups between 51 and 54 breaths/ minute until the end of the experiment. The determined body core temperature progression (Figure 1D) was nearly identical in both groups. It rose from 37.3 °C in the controls and 37.0 °C in the improved nanocapsules group up to 38 °C in both groups at the end of the experiment. Comparison between the two capsule groups revealed significant differences only in MAP (170 and180min after start of the infusion).

Acid base and metabolic status

The pH (Figure 2A) of the improved nanocapsules group was nearly unchanged over the whole experiment at a value of around pH 7.33 whereas the animals of the control group showed a partial drop to pH 7.27 with in the first 30min of the infusion period. An increase to pH 7.32 occurred during the next 60 min and from that time onwards the pH remained stable at this value. The control and improved nanocapsules group showed a decrease of the base excess (Figure 2B) during the period of infusion from around 0mmol/l at the beginning of the experiment to -2.4mmol/l at the end of the infusion. After the infusion, the base excess fluctuated between -0.9 and -2.3mmol/l in both groups. After the infusion the pO2 (Figure 2C) in the animals with the improved nanocapsules stayed at a value around (and in parts higher) 500mmHg and thus permanently above the pO2 in the animals of the control group (about 450 mmHg). The pCO2 showed exactly the opposite behavior, because after the infusion period the pCO2 in the animals receiving the improved nanocapsules was lower (around 45mmHg) compared to the control group with a pCO2 of about 50mmHg. The concentration of blood lactate (Figure 2E) was constant at around 1.5mmol/l in the control group, whereas the animals of the improved nanocapsules group showed an increase of about 2.2mmol/l after an experimental period of 150min. The glucose concentration (Figure 2F) in the control group was around 180mg/dl whereas in the animals of the improved nanocapsules group a decrease of the glucose concentration started at about 90min to reach a final value of 149mg/dl. Comparison between the two capsule groups revealed significant differences only in base excess (0, 60, 120 and 150min after start of the infusion).

Organ/tissue damage

Infusion of HSA 5% did not affect plasma activities of the enzymes ALAT, ASAT and CK (Figure 3A-3C). LDH showed a slight but not relevant decrease at the end of the experiment (Figure 3D) in the control group. However, plasma activities of ALAT (2 fold), ASAT (3.7 fold), CK (3.8 fold) and LDH (3.2 fold) in the improved nanocapsules group were elevated if compared to the HSA 5% group at the end of experiment. Comparison between the two capsule groups revealed significant differences only in ASAT (180 min after start of the infusion) and LDH (150 and 180min after start of the infusion), respectively.

Circulatory in-vivo half-life

The circulatory in-vivo half-life of the improved nanocapsules was calculated to be 170min (Figure 4). At the end of the experiment (180min after start of the infusion) 52.9% of the improved nanocapsules were eliminated from the vascular system.

Discussion

The capsule diameter

In the present study capsules with a significantly reduced mean hydrodynamic diameter (from previously 650nm to now 252nm) and a narrower size distribution, compared to the ones used in previous studies [12], were confected in order to successfully increase the circulatory in-vivo half-life and to reduce side effects.

Effects on systemic parameters

As expected from our previous work [12] the infusion of improved nanocapsules was additionally well to legated by all animals during the experiment. In general the application did not imply dramatic changes in the recorded systemic parameters. Overall, PFC-based artificial oxygen carriers are known for transient systemic hypotension [15,16]. This also was confirmed for capsule-based PFC-containing systems with other wall materials than albumin [14,17]. Most importantly, the presented second and first generation of our nanocapsules only showed a very slight decrease of the MAP within the physiological range (80-120mmHg) after the infusion (Figure 1A). As expected from our study with albumin derived per fluorocarbon-based artificial oxygen carriers of the first generation, the improved nanocapsules, likewise with an albumin shell, prevented additionally systemic hypotension. The slight increase in the heart rate, compared to the control group, again within the physiological range, could be caused by the supply with oxygen (Figure 2C) after treatment with nanocapsules.

Effects on acid base and metabolic status

As expected, the improved nanocapsules operated as an artificial oxygen carrier in animals because an increase of pO2 compared to the animals of the control group was clearly evident (Figure 2C). With regard to the capsules of the first generation we could not observe any difference in the pO2 level [12]. In addition, the improved nanocapsules are able to remove carbon dioxide more effectively as demonstrated by the lower pCO2 compared to the control animal group (Figure 2D). Again, a nearly identical effect was observed with the nanocapsules of the first generation.

Considering the glucose concentration, the application of first and second generation nanocapsules slightly decreased the glucose concentration (Figure 2F) [12]. Excess glycolysis could be the reason for that observation and this rationalization is supported by a corresponding slight lactate increase [18].

The animals of both the control group and the ones receiving the first generation nanocapsules, showed a clear decline in pH after the infusion. In contrast, the application of the second capsule generation did not lead to a decrease outside the physiological pH range (Figure 2A). That indicates a positive influence on the acid base status due to the improved nanocapsules.

The base excess in the control and improved nanocapsule group dropped to -2.4mmol/l but remained in the physiological range between -3 to +3mmol/l (Figure 2B). In our previous study the base excess fell below -4mmol/l (and therefore out of the physiological range) when the animals received the first generation nanocapsules [12]. Particularly regarding the base excess, the improved nanocapsules again performed better than the first generation.

Effects on Organ/tissue damage

Although the infusion of the second generation nanocapsules improved the acid base parameters, the organ tissue damage remained at similar level [12] (Figure 3).

Effects on circulatory in-vivo half-life

One major goal of developing a second nanocapsule generation was to increase the circulatory in-vivo half-life. The first generation of nanocapsules displayed a circulatory in-vivo half-life of 158min [12]. In contrast, the second nanocapsules generation reached a 12min longer circulatory in-vivo half-life of 170 min (Figure 4).

Conclusion

In this study albumin-derived per fluorocarbon- based artificial oxygen carriers were successfully improved with the result of a smaller capsule size. The second nanocapsules generation showed a good biocompatibility in a toxicological screening in an intravenous infusion model in the rat. As expected and with respect to their final destination a better oxygen supply compared to the control group could be recognized. Compared to the nanocapsules of the first generation [14] the nanocapsules of the second generation showed partially a better biocompatibility, especially in the field of acid base status was an improved result observed. Worth mentioning as well is the longer circulatory in- vivo half-life for the second generation nanocapsules without deterioration in biocompatibility. To sum up, the second generation albumin-derived per fluorocarbon-based artificial oxygen carriers showed slightly better biocompatibility and a longer circulatory in-vivo half-life than the first generation nanocapsules analyzed previously. The actually observed improvements are rather small but clearly indicate that the size reduction of the capsules successfully yielded in an increased circulatory in-vivo half-life and a reduction of side effects. Thus, therapeutic application of the improved nanocapsules is already conceivable even if more steps of optimization might be necessary.

Acknowledgment

We thank Prof. Matthias Epple (Institute of Inorganic Chemistry, University of Duisburg-Essen, Germany) for providing the Zetasizer ZS, Malvern Instruments