- Open Access
Mitigating prolonged QT interval in cancer nanodrug development for accelerated clinical translation
© Ranjan et al.; licensee BioMed Central Ltd. 2013
- Received: 14 October 2013
- Accepted: 11 December 2013
- Published: 14 December 2013
Cardiac toxicity is the foremost reason for drug discontinuation from development to clinical evaluation and post market surveillance [Fung 35:293-317, 2001; Piccini 158:317-326 2009]. The Food and Drug Administration (FDA) has rejected many potential pharmaceutical agents due to QT prolongation effects. Since drug development and FDA approval takes an enormous amount of time, money and effort with high failure rates, there is an increased focus on rescuing drugs that cause QT prolongation. If these otherwise safe and potent drugs were formulated in a unique way so as to mitigate the QT prolongation associated with them, these potent drugs may get FDA approval for clinical use. Rescuing these compounds not only benefit the patients who need them but also require much less time and money thus leading to faster clinical translation. In this study, we chose curcumin as our drug of choice since it has been shown to posses anti-tumor properties against various cancers with limited toxicity. The major limitations with this pharmacologically active drug are (a) its ability to prolong QT by inhibiting the hERG channel and (b) its low bioavailability. In our previous studies, we found that lipids have protective actions against hERG channel inhibition and therefore QT prolongation.
Results of the manual patch clamp assay of HEK 293 cells clearly illustrated that our hybrid nanocurcumin formulation prevented the curcumin induced inhibition of hERG K+ channel at concentrations higher than the therapeutic concentrations of curcumin. Comparing the percent inhibition, the hybrid nanocurcumin limited inhibition to 24.8% at a high curcumin equivalent concentration of 18 μM. Liposomal curcumin could only decrease this inhibition upto 30% only at lower curcumin concentration of 6 μM but not at 18 μM concentration.
Here we show a curcumin encapsulated lipopolymeric hybrid nanoparticle formulation which could protect against QT prolongation and also render increased bioavailability and stability thereby overcoming the limitations associated with curcumin.
- QT prolongation
Cardiac safety is very critical for any drug development. Since drug development often takes many years and requires an investment of millions of dollars to achieve FDA approval, it becomes critical to determine the cardiac safety and translational possibilities early in the development process[1–5]. In the early 1990s, several marketed drugs were withdrawn due to their arrhythmogenic risk. On a standard ECG, these drugs prolonged the QT interval which is the duration measured from the beginning of the QRS complex (depolarization of the cardiac myocytes) to the end of the T wave (completion of the repolarization phase of the cardiac myocytes). A prolonged QT interval may potentially induce torsade des pointes (TdP) which is a form of ventricular arrhythmia. Repolarization of the cardiac action potential is a result of currents generated by an outward flow of K+ through the K+ channels. Obstruction of ion flow in the channel leads to delayed repolarization as evidenced by a prolonged QT interval. This led the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use to issue the E17 guideline in 2005. This guideline was directed at the clinical evaluation of QT interval prolongation and proarrhythmic potential of non-antiarrhythmic drugs. During drug development and phase I-II studies, it is important to ascertain the potential of the drug to cause (a) direct myocyte toxicity, (b) changes in cardiac repolarization, (c) prolong QT interval, (d) effects on vascular tone and injury, or (e) induction of life threatening proarrhythmias. The guideline required that the effect on cardiac repolarization of every drug, including anticancer agents, should be evaluated before phase II trials.
Several drugs can interfere with hERG (human ether-a-go-go-related gene) coded potassium channels, which are responsible for the rapid component of repolarisation. This drug induced inhibition may ultimately lead to prolongation of the QT interval. The hERG (human ether-a-go-go related gene) encodes for the α-subunit of the ion channel that is responsible for the rapidly activating delayed rectifier potassium channel IKr (Kv11.1). The three-dimensional structure of the hERG channel is still unknown although site-directed mutagenesis data have provided some insight into its structure. Within the hERG channel pore cavity, ion flux and currents can be modified depending upon the open or closed states, and by drug interactions at key high affinity drug binding sites. These sites are the aromatic amino-acid residues (Y652 and F656) on the inner helices of the pore. The most important currents mediated by drugs are the sensitive delayed IKr (rapid) current which repolarizes the myocardial cells and the IKs (slow) rectifier currents are exhibited on the standard ECG as the QT interval. The corrected current with heart rate is defined as QTc. This IKr or the hERG current is critical for ventricular repolarization and inhibition of IKr can induce QT prolongation which may result in life threatening ventricular arrhythmias.
Curcumin is a drug molecule that has an enormous clinical potential as a potent anti-cancer, anti-oxidant, anti-inflammatory and anti-bacterial drug in addition to its many other pharmacological properties. Unfortunately, curcumin has been reported to block the hERG K+ potassium channel[7, 13]. Studies revealed that curcumin inhibited the hERG K+ channel in a concentration dependent manner with an IC50 as low as 5.5 μM. A low concentration of 11.4 μM of curcumin resulted in an 80% inhibition of hERG tail current density leading to prolongation in the QT interval. Since curcumin induces QT prolongation, it is unsafe for clinical translation unless there are ways to inhibit its QT prolonging properties. Until now there has been only one study on QT prolongation caused by curcumin. This particular study shows that liposomal formulation of curcumin is able to prevent QTc prolongation. However, the concentration of liposomal curcumin which is able to provide this protection is still much lower than the therapeutic concentration.
E-4031, a class III anti-arrhythmic drug is a synthetic toxin used solely for research with one clinical exception. Its mechanism of action is to block the hERG voltage-gated K+ channels. E-4031, purchased from Sigma-Aldrich, was selected as a positive control compound for this study. Three naive HEK293-hERG cells were exposed to 100 nM E-4031.
Curcumin, 99.2% pure, was synthesized under GMP conditions by Sabinsa (NJ, USA) and obtained through SignPath Pharma Inc. The GMP grade liposomal curcumin was obtained from Polymun GmbH (Vienna, Austria). The liposomal curcumin were made with a 9:1 ratio of DMPC (1,2-dimyristoil-sn- glycero-3-phosphocholine) and DMPG (1,2-dimyristoyl-sn-glycero-3-phospho-rac-[1-glycerol]) with a curcumin content of 6.4 mg/ml.
The concentration of various curcumin nanoformulations and curcumin (6, 12 and 18 μM) were selected based on predicted human plasma levels. The selected concentrations reflected a range estimated to exceed the therapeutic doses and provide valuable predictions of the effect of curcumin and various nanocurcumin formulations on human cardiac electrophysiology.
Formulation of lipopolymeric hybrid curcumin nanoparticles
Three different formulations of curcumin encapsulated lipopolymeric hybrid nanoparticles were prepared to identify the best suited formulation.
Formulation A (HNC-NP): nanoprecipitation
Curcumin was dispersed in an organic phase containing PLGA in acetonitrile. The lipids, DMPC (1,2-dimyristoil-sn- glycero-3-phosphocholine) and DMPG (1,2-dimyristoyl-sn-glycero-3-phospho-rac-[1-glycerol]) were used at a pre-determined ratio (7:3). There are previous reports of liposomes composed of the same lipids (i.e. DMPC and DMPG), which lacked general toxicity and decreased nystatin toxicity. Hence we chose to use the same combination of lipids but optimized the ratio in a previous study to obtain the optimal formulation. DMPG was dissolved in double distilled water while DMPC was dissolved in 4% ethanol water. Both lipids were then mixed and heated to 45°C. The organic phase mixture was subsequently added dropwise with constant stirring. The mixture was stirred for 3 hours on magnetic stirrers to facilitate evaporation of the organic solvent from the formulation. Once the organic solvent was evaporated, the mixture was centrifuged thrice at 6000 rpm for 15 minutes using Amicon filters with a 10 kd cutoff. The nanoparticles so obtained were resuspended in a 5% sucrose that acts as a cryoprotectant. Further, the nanoparticle-cryoprotectant mixture is flash frozen in liquid nitrogen for 5 minutes and then lyophilized overnight.
Formulation B (HNC-PS): probe sonication
Curcumin was dispersed in an organic phase containing PLGA in ethyl acetate. The lipids, DMPC (1,2-dimyristoil-sn- glycero-3-phosphocholine) and DMPG (1,2-dimyristoyl-sn-glycero-3-phospho-rac-[1-glycerol]) were used in the same ratio (7:3). DMPG was dissolved in double distilled water while DMPC was dissolved in 4% ethanol water. The lipid mixture and the PLGA-curcumin solution were mixed and sonicated for 1 minute. Subsequently, the nanoparticles were centrifuged at 6000 rpm for 15 minutes using Amicon filters with a 10kd cutoff and then washed thrice. The nanoparticles were resuspended in a 5% sucrose, flash frozen in liquid nitrogen and lyophilized overnight.
Formulation C (HNC-PS-C): probe sonication with chitosan blended polymer
In this protocol, chitosan was added during the formulation of curcumin loaded PLGA nanoparticles using ethyl acetate by solvent evaporation in order to provide a positive surface charge to the nanoparticles. Since lipids mostly carry negative charge, this method leads to a tighter lipid layer on the surface of the nanoparticles. The formulation was carried out as described under probe sonication.
Characterization of lipopolymeric hybrid curcumin nanoparticles
The lipopolymeric hybrid nanocurcumin from all three batches were characterized for their drug loading as previously described. Particle size and zeta potential are important parameters as they have an effect on both the intracellular uptake as well as the stability of the nanoparticles. Average particle sizes of the nanoparticles were determined by Nanotrac Particle Size Analyzer (Mircotrac, Inc., Montgomeryville, PA). Nanoparticles were characterized for zeta (ζ) potential by using a Zetasizer (ZEN4602, Malvern Instruments, Worchestershire, UK). The dried nanoparticles were suspended in distilled Milli Q treated water (pH 7) and measured. Zeta potential was calculated based on electrophoretic mobilityof the nanoparticles in aqueous medium. Surface morphology was determined by Transmission Electron Microscopy (TEM) as described elsewhere. Further, stability analysis was also carried out at 4°C for all the three batches of nanoparticles formulated.
Determination of hERG current inhibition
The compounds tested for hERG current inhibition include lipopolymeric hybrid nanocurcumin (HNC-NP, HNC-PS, HNC-PS-C), liposomal curcumin and curcumin. E-4031 was selected as the positive control to confirm the sensitivity of the test system. This study was carried out at IPS Therapeutique, Inc., QC, Canada.
Manual patch clamp assay
Whole cell patch-clamp recordings were made at 35 ± 2°C from HEK 293 cells stably transfected with the hERG gene. Cells were plated onto 35 mm petri dishes (Falcon) and maintained in culture with the selective agent G148 (Sigma-Aldrich, St. Louis). Cells were washed twice with 1 mL of hERG external solution containing (mM) NaCl 140, KCl 5, CaCl2 1.8, MgCl2 1, Glucose 10 and HEPES 10 (pH 7.4) followed by the addition of 2 mL of hERG external solution. The petri dish (experimental chamber) was mounted on the stage of an inverted phase contrast microscope. A borosilicate glass micropipette (open resistance of 5 to 15 MΩ) pulled with a PMP-102 Programmable Micropipette Puller and filled with internal pipette solution containing (in mM) KCl 140, MgCl2 1, EGTA 5, HEPES 10, Mg-ATP 4 and sucrose 10 was positioned above a single cell using an Eppendorf PatchMan micromanipulator. The micropipette was lowered to the cell until a close contact was achieved. The whole-cell configuration was then obtained by applying a slight negative pressure (resistances were measured by a 5-mV square pulse to be in the GΩ range). Cell capacitance was immediately measured in order to evaluate cell surface area, using a conversion factor of 1 pF/m2. This cell surface area was later used to calculate net current density (as opposed to current amplitude).
Currents were acquired at a rate of 1 kHz, and filtered using a low-pass 4-pole Bessel filter with the cut-off rate set at 500 Hz. Baseline condition currents were recorded using the PClamp 10 acquisition suite (Molecular Devices, Sunnyvale, CA) following a 2-minute equilibration period. Currents were then recorded after 5 minutes of exposure to each concentration of test compounds or positive controls (lipopolymeric hybrid nanocurcumin, liposomal curcumin, curcumin, E-4031). The cells were stimulated continuously with the following pulse:
Currents were analyzed using the Clampfit 10.2.0.14 module of the pClamp 10.2.0.14 software (Axon Instrument Inc., Foster City, California, USA, (now Molecular Devices Inc.).
Current run-down and solvent effect correction
All data points have been corrected for solvent effect and time-dependent current run-down. Current run-down and solvent effects were measured simultaneously by applying the experimental design in test-compound free conditions (dimethyl sulfoxide vehicle) over the same time frame as was done with the test compounds. The loss in current amplitude measured during these vehicle control experiments (representing both solvent effects and time-dependent run-down) was subtracted from the loss of amplitude measured in the presence of the test compound. This procedure isolates the effect of the test compound from the effect of the solvent and the inevitable run-down in current amplitude over time.
Application of test compounds, positive control and vehicle
Cells were exposed for 5 minutes to each concentration of compounds in the presence of closed circuit perfusion (2 mL/min). The cells were allowed 5 minutes for washout in the presence of a flow-through perfusion (2 mL/min) in addition to a closed circuit perfusion (2 mL/min). The positive control (100 nM; E-4031) was added to naive cells obtained from the same cell line and passage number for a period of 5 minutes in presence of a closed circuit perfusion (2 mL/min). Cells were under continuous stimulation of the pulses protocol throughout the experiments and cell currents were recorded after 5 minutes of exposure to each condition.
Statistical comparisons were made using paired Student’s t-tests. For the test compounds, the currents recorded after exposure to the different test compound concentrations were statistically compared to the currents recorded in baseline conditions. Currents recorded after the washouts were compared to the currents measured after the highest concentration of test compounds. In the same way, currents recorded after the positive control was compared to the currents recorded in baseline conditions. Differences were considered significant when p ≤0.05.
Formulation and characterization of lipopolymeric hybrid curcumin nanoparticles
Effect of different formulations on whole-cell IKr hERG currents
The hERG assay or the Manual Patch Clamp assay is used to assess the potential of a compound to interfere with the rapidly activating delayed-rectifier potassium channel. This inital study used stably transfected Human Embryonic Kidney cells (HEK 293 cells) in normoxic conditions to quantify the in vitro effects of lipopolymeric hybrid nanocurcumin formulations, (HNC-NP, HNC-PS and HNC-PS-C), liposomal curcumin and free curcumin on the potassium-selective IKr current. The study design was based on the current International Conference on Harmonisation (ICH) Harmonized Tripartite Guidelines.
Effect of tested compounds on hERG current density at +20 mV (I +20 )
Statistically significant inhibition starting at (μM)
Maximal inhibition (%)
Statistically significant reversibility of the Washout
Calculated IC50 (μM)
It has been previously reported that curcumin interacts with the alpha subunit of the K+ channel which forms the pore of the hERG channel. It is this subunit which is encoded by the hERG gene. Maati et al reported a similar study showing that a curcuminoid mixture containing 78% curcumin brought about comparable inhibition of the hERG current. A study by Helson et al demonstrated that liposome may have a protective effect against the inhibitory interactions of active compounds with channel drug receptor sites allowing more normal gating kinetics to occur. However, they could not confirm whether the changes in gating kinetics were due to a direct interaction of curcumin with the pore-forming peptides, or whether a change in lipid packing in proximity of the hERG channel resulted in decreased inhibition. However, the concentration of liposomal curcumin which is able to provide this protection was much lower than the therapeutic concentration of curcumin and the liposomal formulation was found to be stable only at -20°C.
The results of the present study (Table 1) confirm that the curcumin (diferuloylmethane) molecule exhibits prominent IKr inhibition as reported by other research groups[7, 13]. In the present study, our formulation of lipopolymeric hybrid nanocurcumin formulation was conceptualized based on the protective effects of liposomes on curcumin dependent inhibition of the hERG current. Further, the introduction of a polymer layer in the hybrid formulation imparted much needed stability and tunability to the formulation. The manual patch clamp assay of HEK 293 cells clearly illustrated that this hybrid nanocurcumin formulation prevented the curcumin induced inhibition of hERG K+ channel at concentrations higher than the therapeutic concentrations of curcumin. Liposomal curcumin, on the other hand, could only decrease this inhibition at lower curcumin concentration (6 μM). Comparing the percent inhibition, the hybrid nanocurcumin limited inhibition to 24.8% at a high curcumin equivalent concentration of 18 μM (n = 3; statistically significant). This is substantially less than the inhibition (30%) brought about by liposomal curcumin at one third the concentration (6 μM curcumin equivalent). There remains a need to determine whether the changes in gating kinetics were brought about due to direct interaction of curcumin with pore-forming peptides, or whether a change in lipid packing in proximity of the hERG channel resulted in decreased inhibition. Moreover, the present formulation provided improved bioavailability (data not shown) and as expected, this formulation was stable both at 4°C for an extended period of time.
The inhibition of the IKr current induced by curcumin is mitigated when curcumin is incorporated within a lipopolymeric hybrid nanoparticle formulation prior to exposure. Such a formulation not only protects inhibition of hERG channel current induced by curcumin but also provides improved bioavailability and stability. Similar hybrid formulations may be used for other QT-prolonging drugs to mitigate prolonged QT effects in vitro. Further testing of the hybrid nanoformulation with other QT-prolonging drugs in animal models with QT-prolongation may lead to faster clinical translation and FDA approval of such cardiotoxic yet pharmacologically potent drugs.
Authors would like to thank Dr M Majeed CEO of Sabinsa for contributing GMP grade curcumin. Authors would also like to thank A. Brun and the Microscopy core facility at UNTHSC for technical help in performing the TEM studies. Authors would also like to thank A. Bouchard at IPS Therapeutique, Inc., QC, Canada for experiments and discussions related to the hERG assay. This research was supported by a Sponsored Research Agreement from SignPath Pharma Inc., PA, USA.
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