C.
Fenzl
a,
C.
Genslein
a,
C.
Domonkos
b,
K. A.
Edwards
c,
T.
Hirsch
a and
A. J.
Baeumner
*ac
aInstitute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, Universitaetsstr. 31, 93053 Regensburg, Germany. E-mail: antje.baeumner@ur.de
bResearch Centre for Natural Sciences, Hungarian Academy of Sciences, Magyar tudósok körújta 2, 1117, Budapest, Hungary
cDepartment of Biological and Environmental Engineering, Cornell University, Riley-Robb Hall, 111 Wing Drive, Ithaca, NY 14853-5701, USA
First published on 15th June 2016
Nanoparticles are ubiquitously used for signal enhancement in (bio)sensors, but their true possible performance is typically hampered by non-specific binding. A better understanding of the nature and the prevention of non-specific binding through surface engineering of the particles and sensor surfaces is needed to intelligently design (bio)sensors and potentially avoid bulk blocking methods. Hence, two types of liposomes were used as model for signal-enhancing nanoparticles. Their surface was engineered to bear negative surface charge. One type was synthesized with additional 6 mol% –COOH groups. Their interaction with four typical chemically modified sensor surfaces was then mechanistically characterized by surface plasmon resonance (SPR) spectroscopy. It was shown that the non-specific binding can be described with Langmuir isotherms providing quantitative information of dissociation constants and surface loading with especially high correlation coefficients (>0.97) for all the studied sensor surfaces modified with hydrophilic alkane thiols. By tailoring the sensor surface chemistry, non-specific binding was significantly minimized. Here, carboxyl- or methyl-terminated surfaces performed best. In fact, the pairing of –COOH groups on the sensor surface with –COOH groups on the liposomes almost completely eliminated non-specific binding, resulting in a SPR signal change of only 1 mRIU (refractive index unit) at 100 μM phospholipid concentration. Surprisingly though, –OH groups on the surface, which are also commonly used in sensing applications, did not lead to decreased adsorption, but caused significant signal changes (4 mRIU at 100 μM phospholipid) due to non-specific binding. Overall, the mechanistic studies presented here demonstrate that by careful design of the nanoparticle surface and by choosing sensor surfaces with terminal –CH3 or –COOH groups, improved sensing (micro)systems with very low non-specific adsorption can be obtained.
Despite the high performance of liposome-based sensors and drug delivery systems, the dynamics of the interactions between the utilized vesicles and their target surfaces have only been marginally studied and are still not well understood. In particular, in microfluidic devices – a growing field in (bio)analytical research – high surface areas are encountered that can lead to increasing non-specific adsorption15 and need to be avoided by clever surface engineering strategies. Here, mechanistic understanding of the binding processes is crucial for the optimization of sensors as well as therapeutic applications based on liposomes, where intensive efforts in liposome engineering are made to maximize the uptake of a drug for the desired target.7 Therefore, it is of high importance to know how much, how fast and how strong the vesicles bind to the target surface specifically and non-specifically.
Liang et al.16 investigated the effect of flow rate and water content on targeted liposome interactions via surface plasmon resonance (SPR) spectroscopy and quartz crystal microbalance (QCM) studies. They found that increasing the flow rate decreases the maximum amount of bound liposomes and the equilibrium constant, as does decreasing the water content in the bound vesicle layer. Further, the morphology of the lipid layer on a surface can be controlled by the surface chemistry on the substrate.17 Granqvist et al.17 showed that low-molecular-weight dextran-based surfaces facilitate the formation of supported lipid bilayers, whereas polyethylene glycol-based thiol-surfaces lead to supported vesicular layers. These findings are of high importance when using liposomes as carriers for drugs6,18 or signal molecules10 that should be released in a controlled manner. Recently, Calver et al.19 were able to monitor lipid membrane–surface interactions such as liposome adsorption and deformation using single-particle fluorescence of conjugated poly[5-methoxy-2-(3-sulfopropoxy)-1,4-phenylene-vinylene] on SiO2 nanoparticles.
Extensive studies of lipid vesicle adsorption and supported lipid bilayer formation have been performed by the groups of Reviakine,20,21 Richter and Brisson,22,23 and Kasemo.24–26 They studied the behaviour of liposomes on sensor substrates such as SiO2,24–26 TiO2,20,25 gold24–26 or mica22,23 that contributed significantly to the general understanding of liposome binding to standard sensor substrates of SPR, QCM and atomic force microscopy and the conditions for bilayer formation.
However, again, studies are missing that investigate binding interactions with the predominant surface modifications applied in (bio)analytical assays and sensors, e.g. surfaces modified with terminal carboxyl or hydroxyl groups.14,27 Yet, this knowledge will lead to viable surface engineering strategies that contribute to higher selectivity and reusability, as the commonly used bulk blocking with proteins or polymers is often not sufficient enough to prevent non-specific binding completely. In addition, the liposome formulations used in the previous studies differ clearly from those used in high-performance sensing approaches.1,14,28 As the composition influences sensing performance it must also be used when trying to understand and thereby minimize non-specific binding.
Here, we present the systematic study of non-specific binding interactions between highly stable anionic liposomes and surfaces with varying surface charge and hydrophilicity (Fig. 1). We focus on this type of liposome, as it is favourably used in high-performance sensing applications1,10 that are often combined with microfluidic sample handling.15,29 Liposomes with negative surface charge have been shown not to rupture as easily as positively charged ones when adsorbing to solid surfaces.30 Also, with most biological molecules bearing negative charges, non-specific binding of anionic liposomes favours their use in bioassays. The vesicles were characterized in close detail regarding size and surface charge. The binding studies were performed using SPR spectroscopy that has been shown to be the ideal tool for label-free monitoring of such interactions in real-time resolution.16,17,31 Further, the influence of various temperatures on the binding behaviour was analysed. With our present work, we will broaden the knowledge on liposome–solid surface interactions; this will benefit a wide range of applications by providing clever surface engineering strategies preventing non-specific adsorption without the need of bulk blocking or surface coating.
Fig. 1 Sensing scheme for the interactions between anionic liposomes and different self-assembled monolayers on gold. High non-specific binding will result in high SPR signal changes. |
Then, the solution was sonicated for 1 min in a sonication bath (Bandelin Sonorex Digitec DT 255 H) at 45 °C for homogeneous mixing. A 45 °C salt solution (2 mL of 300 mmol L−1 NaCl) was added to the lipid mixture and then again sonicated for 4 min. The organic solvent was removed at 45 °C and 380 mbar for 20 min using a rotary evaporator. The mixture was vortexed before and after a second addition of 2 mL 45 °C 300 mmol L−1 NaCl. The flask was returned to the rotary evaporator for 20 min at 45 °C and 380 mbar and then for 20 min at 280 mbar. The crude liposome dispersion was further extruded at 50 °C 21 times through 1.0 μm Nucleopore membranes (Whatman, Florham Park, NJ, USA), followed by 21 times through 0.4 μm membranes. The liposomes were purified via size-exclusion chromatography with a Sephadex G-50 in a 15 × 1.6 cm column at ∼4 mL min−1 using HEPES-saline-sucrose buffer (HSS; 10 mmol L−1 HEPES, 200 mmol L−1 sodium chloride, 200 mmol L−1 sucrose, 1.5 mmol L−1 sodium azide at pH 7.5). The fractions containing liposomes were combined and dialyzed overnight against HSS before storage at 4 °C.
The electrophoretic mobility of the liposomes was measured with 1:100 dilution in HEPES-saline buffer. A Folded Capillary Cell (Malvern DTS1070) was charged with approximately 800 μL of the liposome dispersions and equilibrated to 25 °C for 120 s. The mean electrophoretic mobility was determined by laser Doppler velocimetry with the Zetasizer nano series. The Smoluchowski model was employed to determine the zeta potential of the dispersions.34
For the determination of the phospholipid concentration of liposomes, inductively coupled plasma-atomic emission spectroscopy (ICP-AES) was used. A volume of 20 μL of liposomes was diluted in HNO3 (c = 0.5 mol L−1) to a total volume of 3 mL. The mixture was vortexed and sonicated thoroughly. Phosphorus standard solutions were prepared with concentrations of 1, 5, 10, 25, 50 and 100 μmol L−1 phosphate in 0.5 mol L−1 HNO3 for calibration. The phosphorus content was measured via ICP-AES (Spectro Flame-EOP, Analytical Instruments GmbH, Kleve, Germany) at the phosphorus specific wavelength of 178.29 nm.
Liposomes were characterized with respect to their size and surface charge. Dynamic light scattering was used to determine their hydrodynamic diameters. The non-tagged liposomes had a diameter of 170 nm, with a polydispersity index (PDI) of 0.16. Liposomes with N-glutaryl-1,2-dipalmitoyl-sn-glycero-3-phosphatidylethanolamine (N-glutaryl-DPPE) are 240 nm in diameter (PDI of 0.22). The carboxylic groups providing additional negative surface charge as well as additional sodium counter ions can cause – among other synthesis parameters – such an increase in hydrodynamic diameter.35 Glutaryl-tags on the liposome surface lead to higher electrostatic repulsion between the liposomes. As a consequence, the incorporation of charged tags in the bilayer membrane contributes to improved colloidal stability. Furthermore, the higher surface charge can indeed enhance the colloidal stability in solution due to stronger repulsion between the nanovesicles, yet it can also increase binding to the surfaces of opposite surface charge, which needs to be considered when designing the overall sensor setup.
The zeta potential obtained by electrophoretic mobility measurements of –COOH-tagged liposomes (−47 ± 3 mV) is more negative than for the untagged ones (−34 ± 3 mV). Both types of liposomes show extreme long term stability and keep their physical and hydrodynamic diameters as well as the high negative zeta potential for at least 400 days.36 This exceeds by far the colloidal stability of numerous other nanomaterials such as polystyrene nanospheres37,38 or magnetite nanoparticles.39
Transmission electron microscopy (TEM) images show the successful formation of the liposomes that display good regularity of size and shape (Fig. 2). Deviations from the perfectly spherical shape of liposomes on the images are likely due to the drying and staining process on the TEM grid.
Fig. 2 TEM images of a 1:10 diluted dispersions of untagged liposomes (left) and liposomes with the N-glutaryl-DPPE tag (right). Scale bars represent 500 nm. |
The phospholipid concentration was determined via ICP-AES resulting in 6.14 ± 0.12 mmol L−1 for the untagged batch and 11.17 ± 0.13 mmol L−1 for the liposomes with the N-glutaryl-DPPE tag. The total lipid concentration can be calculated using the molar ratios of the lipid composition (see the Experimental section) to be 11.3 ± 0.2 and 19.7 ± 0.2 mmol L−1, respectively. The total number of lipids per liposome is given by eqn (1):40
Ntot = (π/aL)[d2 + (d − 2t)2] | (1) |
The successful formation of closely packed alkanethiol monolayers on gold provides an insulation barrier43 for the hexacyanoferrate and can be seen in a drastic change of the redox peaks in the cyclic voltammograms (CV) (Fig. S1†). Starting with clearly defined reduction peaks between +310 and +340 mV (vs. Ag/AgCl) and oxidation peaks between 0.05 and 0.12 mV for unmodified gold electrodes, all four different thiols show successful formation of a self-assembled monolayer (SAM) on the gold electrodes, as the surface is blocked for the redox reaction and the redox currents are significantly decreased, resulting in CVs without clearly discernible peak potentials. The best blocking is exhibited by the CH3-terminated thiol monolayer, followed by the –COOH- and –OH-modified surfaces. For the electrode modified with 11-mercaptoundecyl amine hydrochloride a hindered charge-transfer can be seen by the large separation of the peak potentials, indicating the formation of a monolayer.
The binding curves were fitted to the extended Langmuir model following eqn (2):
(2) |
Positively cooperative binding is given by h > 1, and negatively cooperative binding by h < 1. For non-cooperative binding h is equal to 1. The fitting parameters are displayed in Tables S1 and S2† for both the simple Langmuir model (h fixed to 1), which neglects cooperative binding effects, and for the extended fit, which takes such effects into account. The Langmuir model was chosen over the Freundlich isotherm, as the experimental data display saturation behaviour.
The non-specific binding of anionic liposomes to varying surfaces can be mainly classified into two parameters: the total refractive index change at a certain liposome concentration and the binding affinity. Liposomes strongly bind to an unmodified gold surface resulting in a refractive index change of 0.007 RIU at 453 pM under physiological pH, as shown in Fig. 3. By modifying the gold surface with an amino-terminated monolayer, the binding interaction is even stronger and a signal change of 0.014 RIU can be observed. In the case of 11-mercaptoundecanol monolayers, signals (0.006 RIU) comparable to the unmodified gold were obtained. However, the 11-mercaptoundecanoic acid induces electrostatic repulsion leading to a clear blocking effect (0.003 RIU) which is even stronger for the hydrophobic surface (1-mercaptoundecane) which prevents the hydrophilic liposomes from binding (0.001 RIU).
Regarding the binding affinity, the standard Langmuir isotherms (h = 1) display decreasing dissociation constants with increasing positively charged sensor surface charge starting at KD = 1400 pM for HS(CH2)10–COO− due to the repulsive interactions. The uncharged hydrophilic surface self-assembled by HS(CH2)11–OH results in a lower KD value of 310 pM, whereas for the highly attractive interactions caused by the positively charged surface consisting of a SAM of HS(CH2)11–NH3+, a dissociation constant of 160 pM is obtained. For all hydrophilic surfaces, the refractive index change at maximum surface loading ΔnD, max lies consistently in the same range between 0.01 and 0.02 RIU, indicating a similar surface loading for the three surfaces at infinite liposome concentration. The SAM of the hydrophobic HS(CH2)10–CH3 on the other hand results in a very low ΔnD, max of 0.0013 RIU. This can be explained by the fact that the Langmuir fit is not very accurate for this hydrophobic surface (R2 = 0.85) due to the high differences in polarity between the liposome dispersions and the sensor surface. All other Langmuir fits show R2 values of more than 0.97 assuring the applicability of the model without the need to use more elaborate adsorption isotherms.
The standard Langmuir isotherms do not consider cooperative binding effects, especially for the interaction of positively charged amino groups to negatively charged phospholipids at pH 7.5. In accordance with this, the binding isotherms fitted by an extended Langmuir equation indicate positively cooperative binding for –NH2 SAM, non-cooperative binding in the case of –COOH SAM, negatively cooperative binding for blank gold and –OH SAM (Table S1†). The fitting of –CH3 SAM did not converge for this model, indicating that there is almost no interactions of the liposomes with this surface. In general, the coefficient referring to the cooperative effects is in all cases close to 1, and the precision of the binding constants is significantly lower than those obtained by the simple Langmuir isotherms.
The very strong attractive interactions between the highly negatively charged liposomes with the cationic SAM consisting of HS(CH2)11–NH3+ lead to a high signal change of 0.012 RIU at a liposome concentration of 200 pmol L−1, whereas the uncharged hydroxyl surface results in 0.004 RIU (Fig. 4). Only very small changes can be observed for the interactions to the carboxyl- and the hydrophobic CH3-moiety (0.001 RIU). This is caused by the strong electrostatic repulsion of the first and the significant differences in polarity of the second surface.
As already observed for the untagged liposomes, the dissociation constants obtained from the Langmuir fits of the hydrophilic surfaces with the liposomes with the N-glutaryl-DPPE tag decrease from 400 pM for repulsive interaction of the carboxyl surface, over 330 pM for the 11-mercaptoundecanol to only 70 pM for the strong attractive interactions of the positively charged amino surface. The refractive index change at maximum surface loading lies in the range between 0.01 and 0.02 RIU for the hydroxyl- and amino-terminated surface and is significantly reduced to 0.0052 RIU for HS(CH2)10–COO− due to the strong electrostatic repulsion. The difference in polarity between the liposomes and HS(CH2)10–CH3 is the reason for the very low signal change at a maximum surface loading of 0.0018 RIU and the rather low R2 value of 0.72 for the fit. All other Langmuir fits show R2 values of more than 0.97 assuring the applicability of the model and showing no need of more elaborate fitting curves.
The additional negative surface charges introduced by the N-glutaryl-DPPE phospholipid influence the intra-molecular interactions between the charged liposomes themselves, thus reducing the apparent binding on the surfaces. Therefore, liposomes of the same phospholipid concentration of 100 μM were compared (translating into 453 pM liposome concentration for the untagged batch and 206 pM for the glutaryl-tagged batch), as this is a typical concentration used in analytical applications.14,45 For all surface modifications, except the –CH3 terminated surface, the signal change for the N-glutaryl-DPPE tagged liposomes is lower (Fig. 5). In the case of 11-mercaptoundecane all findings suggest that there is nearly no binding and therefore the signal changes are almost equal. However, the differences between the two types of liposomes are small in comparison with the influence of the modified sensor surface, showing the importance of careful sensor surface engineering for the prevention of non-specific adsorption of liposomes.
Additional –COOH tags provide the possibility of further functionalization and, due to the slightly more negative zeta potential, a better colloidal stability is achieved. In general, the lipid composition of the liposomes is already optimized for long term stability.36 The detailed study of the non-specific binding towards model surfaces, reflecting different chemical functionalities typically present in most biomolecules and sensor substrates, shows that the adhesion of this type of liposome is only weak. Even for positively charged amino surfaces the electrostatic repulsion between the liposomes themselves only leads to a low total surface coverage. Simulation of the binding of such liposomes neglecting their own electrostatic repulsion results in an expected shift in the SPR angle of at least 1.8°. This value is significantly higher than the shift found in the experiment for saturation (0.8°) (Fig. S2†). Liposomes consisting of only zwitterionic phospholipids, as primarily used in the studies by Kasemo et al., show significantly higher non-specific surface adsorption and tend to rupture to form a supported lipid bilayer.24,26 The low non-specific binding is therefore afforded by the overall lower binding ability and has to be taken into consideration in the design of analytical assays, i.e. the highly charged liposomes may ultimately be ideally suited for low analyte concentrations45 and microfluidic testing devices.15,29
The decrease in the overall signal change of liposomes binding to the sensor surface is in accordance with the decreasing refractive index of aqueous solutions with increasing temperature.46 The KD of the liposome binding determined by a simple Langmuir fit decreases between 25 and 50 °C from 310 ± 60 pM to 130 ± 50 pM, indicating stronger interactions between the liposomes and the model sensor surface with increasing membrane fluidity (Fig. S3†). Additionally, this displays the applicability of the Langmuir model over the whole examined range of temperatures.
This is crucial when using liposomes as signal amplification tools,14,15,36,44 as non-specific binding can almost be prevented by modifying the sensor surface with –COOH groups. In addition, the introduction of 6 mol% N-glutaryl-DPPE into the mixed liposome surface reduces non-specific binding even further. This amount is large enough to provide electrostatic repulsion and high colloidal stability, but still small enough that specific binding is not prevented.44 This demonstrates that liposome surfaces can be tailored to a specific (analytical) task. They provide high specific binding on the one hand14 and show minimized non-specific binding to –COOH surfaces without the need of further protein blocking on the other hand, which makes them unique in comparison with other nanoparticle-based amplification systems, where such a surface engineering is by far not as straightforward. Furthermore, hydroxyl groups are known to minimize non-specific bindings, but we demonstrated that liposomes significantly adhere to –OH surfaces. This finding is important especially for miniaturized bioanalytical detection systems, such as microfluidic biosensors based on liposomes15,29 or similar nanoparticles with large surface areas compared to the total volume, where non-specific adsorption can cause significant problems and lead to high background signals and low sensing performance. Here, clever sensor surface engineering providing electrostatic repulsion or opposite polarity enables minimization of non-specific interactions and hopefully will lead, in the future, to intelligently blocked sensor surfaces and not bulk-blocking as customarily done through polymers and proteins. We will further study these conditions by investigations of the specific binding of receptor-modified liposomes to optimized surfaces. These findings herein will have a big impact on the general understanding of liposome and similar nanoparticle interactions and thus strongly contribute in the development of new and the improvement of existing applications using liposomes as drug carriers as well as for signal enhancement in sensing devices, ranging from standard microtiter plate assays to microfluidic point-of-care diagnostic tools.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c6an00820h |
This journal is © The Royal Society of Chemistry 2016 |