Ex Vivo Red Blood Cell Hemolysis Assay for the Evaluation of pH-responsive Endosomolytic Agents for Cytosolic Delivery of Biomacromolecular Drugs

Podsumowanie

A hemolysis assay can be used as a rapid, high-throughput screen of drug delivery systems' cytocompatibility and endosomolytic activity for intracellular cargo delivery. The assay measures the disruption of erythrocyte membranes as a function of environmental pH.

Streszczenie

Phospholipid bilayers that constitute endo-lysosomal vesicles can pose a barrier to delivery of biologic drugs to intracellular targets. To overcome this barrier, a number of synthetic drug carriers have been engineered to actively disrupt the endosomal membrane and deliver cargo into the cytoplasm. Here, we describe the hemolysis assay, which can be used as rapid, high-throughput screen for the cytocompatibility and endosomolytic activity of intracellular drug delivery systems.

In the hemolysis assay, human red blood cells and test materials are co-incubated in buffers at defined pHs that mimic extracellular, early endosomal, and late endo-lysosomal environments. Following a centrifugation step to pellet intact red blood cells, the amount of hemoglobin released into the medium is spectrophotometrically measured (405 nm for best dynamic range). The percent red blood cell disruption is then quantified relative to positive control samples lysed with a detergent. In this model system the erythrocyte membrane serves as a surrogate for the lipid bilayer membrane that enclose endo-lysosomal vesicles. The desired result is negligible hemolysis at physiologic pH (7.4) and robust hemolysis in the endo-lysosomal pH range from approximately pH 5-6.8.

Wprowadzenie

Although there are many potential high-impact therapeutic targets inside the cell, the intracellular delivery of agents poses a significant challenge. Frequently, drugs, especially biologics, are internalized by cells and trafficked into vesicles that either lead to degradation of their contents through the endo-lysosomal pathway, or are shuttled back out of the cell via exocytosis.¹ In the latter process, the internal pH of the vesicles is acidified to approximately 5-6, which is the optimal pH for activity of enzymes that function in this compartment, such as lysozyme.²

Recently, a number of materials have been specifically engineered to leverage the acidification of endosomes to facilitate cytosolic delivery of their cargo. One example of this approach uses synthetic, polymer micelle nanoparticles whose core is zwitterionic and charge-neutral at physiologic pH (i.e. 7.4). However, at pH 6.0 - 6.5, the polymers become protonated and acquire a net positive charge that destabilizes the micelle core, and the exposed polymer segments interact with and disrupt the endosomal membrane. This activity has been shown to promote the endosomal escape of peptide and nucleic acid-based therapeutics, allowing them to access their cytosolic targets.^3,4 Other examples of methods developed to mediate endosomal escape that disrupt the membrane barrier include 'fusogenic' peptides or proteins that can mediate membrane fusion or transient pore formation in the phospholipid bilayer.⁵ Homopolymers of anionic alkyl acrylic acids such as poly(propylacrylic acid) are another well-studied approach, and in these polymers, the protonation state of pendant carboxylic acid dictates transition into a hydrophobic, membrane-disruptive state in endo-lysosomal pH ranges.^6,7

One useful model system for screening endosomolytic behavior is the ex vivo pH-dependent hemolysis assay.⁸ In this model system, the erythrocyte membrane serves as a surrogate for the lipid bilayer membrane that enclose endo-lysosomal vesicles. This generalizable model has been used by others to evaluate the endosomolytic behavior of cell-penetrating peptides and other polymeric gene delivery systems.^8-11 In this experiment, human red blood cells and test materials are co-incubated in buffers at defined pHs that mimic extracellular (7.4), early endosomal (6.8), and late endo-lysosomal (< 6.8) environments. The amount of hemoglobin released during the incubation period is quantified as a measure of red blood cell lysis, which is normalized to the amount of hemoglobin released in positive control samples lysed with a detergent.

From screening a small library of potentially endosomolytic test materials, one can infer that samples that produce no hemolysis at pH 7.4, but significantly elevated hemolysis at pH < 6.5, will be the most effective and cytocompatible candidates for cytosolic drug delivery. Materials that fit these criteria would be expected to remain inert and not indiscriminately destroy lipid bilayer membranes (i.e. that could cause cytotoxicity) until being exposed to a drop in the local pH following internalization into endo-lysosomal compartments.

In this protocol, erythrocytes are isolated from a human donor and co-incubated at pH 5.6, 6.2, 6.8, or 7.4 with experimental endosomolytic drug delivery agents. Intact erythrocytes are pelleted, and the supernatants (containing hemoglobin released from lysed erythrocytes) are analyzed for the characteristic absorbance of hemoglobin via a plate reader (Figure 1).

Protokół

1. Preparation and Sterilization of Buffers and Test Agents

1. 150 mM NaCl buffer: Dissolve 4.383 g NaCl crystals in 500 ml of nanopure water.
2. pH Buffers: Prepare phosphate buffers at pH 5.6, 6.2, 6.8, and 7.4 by mixing appropriate amounts of monobasic and dibasic sodium phosphate. If samples are to be tested at lower pH values (i.e. pH < 5.6) then a more appropriate buffer, such as citrate buffer, should be used. Buffer recipes are readily available, and an example reference has been provided here.¹²
3. Sterilize all buffers noted above through a bottle-top vacuum filtration apparatus and re-check buffer pH's.
4. 20% Triton X-100 (positive control): Mix 20 ml pure Triton X-100 in 80 ml of nanopure water. Vortex vigorously and sonicate to dissolve. Leave at room temperature overnight before use.

2. Preparation of Erythrocytes

1. Obtain 25 ml of blood from an anonymous human donor, drawn directly into K₂-EDTA-coated Vacutainer tubes to prevent coagulation.

NOTE: All procedures must be pre-approved by the appropriate Institutional Review Board (IRB), and venipuncture and blood collection must be performed by a trained phlebotomist in order to minimize the risk to the donor. Standard phlebotomy procedures have been published elsewhere.¹³

2. Centrifuge blood at 500 x g for 5 min, and mark levels of hematocrit (red, lower layer) and plasma (yellowish, upper layer) on tube.
3. Aspirate plasma gently via a micropipettor, add into bleach, and discard into biohazardous waste.
4. Fill hematocrit tube to marked line (original level of plasma) with 150 mM NaCl solution. Cap and invert a few times to gently mix. Centrifuge at 500 x g for 5 min.
5. Repeat step 2.3-2.4 to wash blood cells again. Then aspirate supernatant and replace with PBS at pH 7.4. Invert to mix.
6. Split blood evenly into four tubes, corresponding to each pH that will be tested. Label the tubes according to each pH to be tested (5.6, 6.2, 6.8, 7.4).
7. Centrifuge blood tubes at 500 x g for 5 min. Mark levels on tubes, then aspirate supernatant.
8. Fill each tube to marked line with buffer of appropriate pH (as indicated in 2.6).
9. Label four 50 ml conical tubes (one per pH to test), and pipet 49 ml of PBS of appropriate pH into each conical tube.
10. Add 1 ml of erythrocytes (same pH) into corresponding tube for a 1:50 dilution. Visually inspect the diluted blood, which should be turbid and will settle if left undisturbed. If no pellet forms, cells have lysed.

3. Lysis Assay 96 Well Plate Setup and Quantification

1. Prepare stock solutions of all experimental drug delivery agents, at 20x the desired final concentration to be tested (Assay will take 10 μl of drug delivery agent + 190 μl diluted red blood cells, leading to a 1/20 dilution of the original drug delivery agent into the final test mixture). Stocks of 20, 100, and 800 μg/ml are suggested, resulting in final test concentrations of 1, 5, and 40 μg/ml, respectively.
2. Pipet 10 μl of each stock solution into V-bottom 96-well plates. For optimal results, load each sample in triplicate or quadruplicate.

NOTE: For ease, it is recommended that a separate 96-well plate should be prepared for each pH to be tested, with each sample (at each concentration) loaded at n=3-4 per plate.

3. For positive control wells, add 10 μl of 20% Triton X-100.
4. For negative control wells, add 10 μl of phosphate buffer. Use buffer at the same pH to be tested.
5. Pipet 190 μl of diluted erythrocytes (see 2.10) to each well, making sure cell stock solution remains homogenous during transfer. Hint: Use multi-channel pipette to simplify this task.
6. Incubate plates at 37 °C for one hour (Optional: Use an orbital shaker or rocker).
7. Centrifuge plates for 5 min at 500 x g to pellet intact erythrocytes. Note: when removing the plate from the centrifuge and transporting it to the next step, handle with care and be certain not to disrupt the cell pellet.
8. Using a multichannel pipet, transfer 100 μl of supernatant from each well into a clear, flat-bottomed 96-well plate. Note: if the cell pellet is accidentally disturbed for any sample(s), one can re-centrifuge the plate and then proceed with supernatant transfer.
9. Measure absorbance of supernatants with a plate reader. Note that a range of wavelengths can be used (400 - 541 nm).

NOTE: Different plate readers may have different saturation points and sensitivities, so the choice of a wavelength for measurements depends on whether or not hemolysis data from experimental samples can be reliably normalized against maximum hemolysis as induced by detergent treatment. This requires accurate measurement of absorbance values of the positive control samples.

10. Using Microsoft Excel or a similar data analysis software, find the average of the background absorbance readings from the negative control samples set up for each pH (step 3.4). Subtract this background absorbance value from all other samples that were measured at that pH.
11. After background subtraction, find the average absorbance of the positive control detergent-treated samples (step 3.3). Then normalize all experimental data points to this mean absorbance value, which should represent 100% hemolysis. Finally, multiply each well value by 100% to calculate % hemolysis that occurred in each individual well relative to the detergent control.

Wyniki

Typically, the agents that exhibit ideal pH-dependent hemolytic behavior have the highest potential for cytosolic delivery of drugs, nucleic acids, or other bioactive molecules. This is exemplified by Agent #1 as portrayed in Figure 2, which exhibits minimal hemolysis at pH 7.4, but a sharp increase in hemolytic behavior at endosomal pH ranges (< 6.5). Some agents may exhibit significant levels of hemolytic behavior at physiological pH ranges (Agent #2 at 40 μg/ml; Figure 2), suggest...

Dyskusje

pH-responsive polymers or other agents designed for endosomolytic function can be rapidly and effectively screened based on lysis of red blood cells at pH values encountered in the endosome (Figure 1; pH 6.8 - early endosome, pH 6.2 - late endosome, pH 5.6 - lysosome).^14-17 pH-dependent hemolysis has been used to screen the ability of carriers to mediate endosomal release of biomacromolecular therapeutics (e.g. peptides, siRNA, ODNs, proteins), and results of this assay can be predict...

Materiały

Name	Company	Catalog Number	Comments
BD Vacutainer - K2EDTA Vacutainer Tubes	Fisher Scientific	22-253-145	For blood collection
BD Vacutainer Blood Collection Needles, 20.5-gauge	Fisher Scientific	02-665-31	For blood collection
BD Vacutainer Tube Holder / Needle Adapter	Fisher Scientific	22-289-953	For blood collection
BD Brand Isopropyl Alcohol Swabs	Fisher Scientific	13-680-63	For blood collection
BD Vacutainer Latex-Free Tourniquet	Fisher Scientific	02-657-6	For blood collection
Hydrochloric acid (conc.)	Fisher Scientific	A144-500	For adjustment of pH of D-PBS.
Triton X-100	Sigma-Aldrich	T8787	Positive control
Dulbecco's PBS	Invitrogen	14190
Nalgene MF75 Sterile Disposable Bottle-Top Filter Unit with SFCA Membrane	Fisher Scientific	09-740-44A
BD 96-well plates, flat-bottomed, tissue culture-treated polystyrene	Fisher Scientific	08-772-2C	For plate-reading at the end of the assay.
BD 96-well plates, round-bottomed, tissue culture-treated polystyrene	Fisher Scientific	08-772-17	For incubation of red blood cells with experimental agents.