Low-Level Detection of Poly(amidoamine) PAMAM Dendrimers Using Immunoimaging Scanning Probe Microscopy

Cason, Chevelle A.; Fabré, Thomas A.; Buhrlage, Andrew; Haik, Kristi L.; Bullen, Heather A.

doi:https://doi.org/10.1155/2012/341260

International Journal of Analytical Chemistry

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Abstract Introduction Experimental Results and Discussion Conclusions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2012 | Article ID 341260 | https://doi.org/10.1155/2012/341260

Low-Level Detection of Poly(amidoamine) PAMAM Dendrimers Using Immunoimaging Scanning Probe Microscopy

Chevelle A. Cason,¹Thomas A. Fabré,¹Andrew Buhrlage,¹Kristi L. Haik,²and Heather A. Bullen¹

Academic Editor: Charles L. Wilkins

Received29 Sept 2011

Accepted03 Nov 2011

Published08 Feb 2012

Abstract

Immunoimaging scanning probe microscopy was utilized for the low-level detection and quantification of biotinylated G4 poly(amidoamine) PAMAM dendrimers. Results were compared to those of high-performance liquid chromatography (HPLC) and found to provide a vastly improved analytical method for the low-level detection of dendrimers, improving the limit of detection by a factor of 1000 ( moles). The biorecognition method is reproducible and shows high specificity and good accuracy. In addition, the capture assay platform shows a promising approach to patterning dendrimers for nanotechnology applications.

1. Introduction

Dendrimers are at the forefront of research in nanoscience due to the many interesting properties of these macromolecular systems including their precise architecture, highly reproducible shape, high uniformity and purity, low immunogenicity and toxicity, high loading capacity, and high shear resistance [1–5]. They have shown a great deal of versatility with applications in numerous areas such as drug delivery [6, 7], gene therapy [8, 9], chemotherapy [10], electrochemistry [11, 12], metal recovery [13], catalysis [14, 15], and sensors [16–18]. Development of new low-level detection and quantification methods is needed with the utilization of these nanomaterials. Currently, high-performance liquid chromatography (HPLC) is the predominate approach reported for dendrimer quantification [19, 20]. However, the primary focus of HPLC, along with capillary electrophoresis, has been to evaluate dendrimer purity and degree of conjugation [21–27]. Little has been reported within the literature with regard to the advancement of new quantification methods for dendrimers.

This work introduces a biorecognition readout technique that has the potential to provide low-level detection of dendrimers. Biotinylated poly(amidoamine) PAMAM dendrimers were chosen as a model target. PAMAM dendrimers, which are highly water soluble, represent the most widely studied class of dendrimers. Functionalization of PAMAM dendrimer surfaces has proven useful in their utilization for various applications including drug delivery and chemical sensing [5, 6, 16]. Biotin-labeled dendrimers have been utilized in tumor [28] and antibody [29] targeting studies and biosensor design [30]. Biotinylated PAMAM dendrimers may also have the potential for delivering therapeutic drugs to the brain [31, 32].

We report here a readout method using an immunoassay platform and scanning probe microscopy (SPM) for low-level quantification of biotinylated G4 PAMAM dendrimers. The assay takes advantage of the documented specificity of biotin-avidin. Results are correlated with HPLC analysis. In addition, we briefly highlight the potential of this capture assay platform to selectively pattern PAMAM dendrimers onto a surface. Patterning of nanoparticles is relevant to a wide variety of applications in the fields of sensing, drug delivery, or development of nanodevices [33–35]. Dendritic architectures show promise in designing and developing sensor platforms with high sensitivity and stability [16].

2. Experimental

2.1. Reagents

Poly(amidoamine) PAMAM dendrimers [core: ethylene diamine] () dendri-PAMAM-(NH₂)₃₂ were obtained from Dendritic Nanotechnologies, Inc. (Mt. Pleasant, MI). Biotinylated PAMAM dendrimers were prepared using sulfo-NHS-LC-biotin (Pierce EZ-Link Kit) as described previously [36]. Briefly, a 3 : 1 molar ratio of biotin/PAMAM dendrimers in 0.1 M phosphate buffer saline (PBS) was allowed to react for 2 h on an orbital shaker. Excess, unreacted biotin was then removed using Microcon filters (Millipore. Bedford, MA, USA). The biotinylation of dendrimers was evaluated using NMR spectroscopy. Biotinylated dendrimers were resuspended (1.0 mg/mL) in 1.0 M PBS until used. Octadecanethiol (ODT), 3,3′-dithio-bis(propionic acid N-hydroxysuccinimide ester) (DSP), bovine serum albumin (BSA), Triton X-100, and avidin >98% were obtained from Sigma (Sigma-Aldrich, St. Louis, MO). Avidin conjugated to Alexa Fluor 488 was purchased from Invitrogen (Invitrogen, Carlsbad, CA). Poly(dimethyl siloxane) (PDMS) was obtained from Dow Corning (Midland, MI). All organic solvents used were analytical, HPLC grade, from Sigma (Sigma-Aldrich, St. Louis, MO). DI water was obtained using a Milli-Q plus water purification system (Millipore, Bedford, MA). PBS and Borate buffers were prepared from Pierce buffer packs (Pierce Protein Research Products, Rockford, IL).

2.2. Capture Substrate Preparation

A modified approach was used for preparation of the capture substrate [37–39] utilizing template-stripped gold (TSG) for SPM imaging, as shown in Figure 1. TSG was prepared by evaporating gold onto p-type silicon wafers (University Wafer) with a resistive evaporator and affixing cm glass pieces (ultrasonically cleaned 30 min each in diluted Contrad 70, DI water, and methanol) using two-part epoxy (Epoxy Technology) followed by curing at 150°C for 2 h. The glass pieces were gently detached from the silicon wafer revealing a smooth gold surface atop the glass chip.

The TSG substrates were exposed for ~30 s to an ODT soaked PDMS stamp (with a 3 mm diameter hole cut in the center), rinsed with ethanol, and dried under high-purity nitrogen. The substrates were then placed in a 0.1 mM solution of DSP in ethanol overnight. The capture platform was then rinsed with ethanol and dried under N₂. This formed the DSP-based adlayer in the areas on the substrate not covered by ODT. The hydrophobic ODT localized reagents in a confined sample area (3 mm ODT spot size) for the capture assay platform.

To form the capture avidin surface, a 20 μL aliquot of avidin solution (500 μg/mL diluted in 50 mM borate buffer) was placed on top of the sample area and allowed to incubate for 6 h at room temperature in a humidity chamber. Substrates were then rinsed with 5 mL of 10 mM PBS (with 0.1% Triton X-100), and the surface area was incubated with a 20 μL solution of blocking buffer (1% (w/v) BSA in 20 mM borate buffer with 0.1% Triton X) for 5 h, followed by rinsing with 5 mL of 10 mM PBS. The capture substrate was then exposed to 20 μL aliquots of various concentrations of biotinylated G4 PAMAM dendrimers diluted in 10 mM PBS for 8 h at room temperature in a humidity chamber. Substrates were then rinsed with 5 mL of 10 mM borate buffer before drying with nitrogen. A blank sample consisted of all stages except the avidin capture surface.

To demonstrate patterning of biotinylated G4 PAMAM dendrimers, a PDMS stamp with a positive structure of 10 μm wide stripes separated by 5 μm was utilized. Preparation of the patterned substrate consisted of all stages, with the following modifications: (1) a sample volume of 200 μL was used instead of 20 μL and (2) after incubation with biotinylated G4 PAMAM dendrimers, the substrate was rinsed with 10 mM PBS and the dendrimers were fluorescently tagged by incubating the substrate with 200 μL of 250 ug/mL of Alexa Fluor conjugated avidin. Following this step the substrates were rinsed with 5 mL of 10 mM borate buffer and dried with nitrogen.

2.3. Scanning Probe Microscopy

A Dimension 3100 Digital Instruments SPM was utilized in tapping mode equipped with 125 μm n-doped silicon cantilevers with resonance frequencies between 110 and 220 kHz and typical scan rates of 0.75–1 Hz (NSC 14, MikroMasch). Typical scan rates were 1 Hz, and all images were acquired in air. For quantification, multiple areas of the capture surface were analyzed and the dendrimers in each μm image were enumerated manually.

2.4. High-Performance Liquid Chromatography

HPLC analysis of G4 biotinylated PAMAM dendrimers was conducted using parameters reported previously [36]. Briefly, a reversed phase HPLC system consisting of a Waters Breeze HPLC (Waters Corporation, Milford, MA, USA), equipped with a 717plus autosampler, 2487 dual λ UV detector, 5 μm Symmetry300 C18 column (), and a Waters Sentry Symmetry C18 guard column was used. The mobile phase consisted of a linear gradient beginning with 90% water and 10% ACN (each with 0.14% TFA) at a flow rate of 1 mL/min reaching 68% water and 32% ACN over 10 minutes. The injection volume was 100 μL, and detection of eluted samples was performed at 214 nm.

2.5. Fluorescent Microscopy

A Nikon E600 fluorescent microscope with a Mercury-100 W light source was utilized to take images at 100x total magnification.

3. Results and Discussion

The principle goal of this work was the development and application of capture platform for quantification of PAMAM dendrimers. A model assay was evaluated using biotinylated G4 PAMAM dendrimers and avidin. Avidin was immobilized onto a patterned thiolate layer, DSP, via succinimidyl ester chemistry (Figure 1). In the presence of biotinylated G4 PAMAM dendrimers, the immobilized avidin layer extracts the dendrimers. SPM analysis of the capture platform revealed the presence of nanometrically sized objects, ~4.5 nm in dimension, according to cross-sectional height profiles. These are consistent in size and shape of G4 biotinylated PAMAM dendrimers, taking into account tip convolution effects (Figure 2). At this scale, the tip convolution effects distorted the resolution in the lateral dimensions, as the dimensions of the particles are smaller than the radius of curvature of the AFM probe used (radius = 20 nm) [40, 41]. The dendrimers largely appear to be captured individually on the platform surface. In some cases dendrimers were found grouped together (2-3 dendrimer clusters) but could be individually distinguished using cross-sectional analysis. SPM analysis reveals that the dendrimers do not have a tendency to cluster together in domains, indicating that sedimentation is not a factor during the incubation. Analysis of control (blank) substrates, devoid of the avidin-specific capture surface, shows limited nonspecific binding ( dendrimers/μm²) and that blocking steps are effective.

(a)

(b)

(c)

(d)

(e)

The patterning of DSP provides a reproducible surface area for quantification. Figure 2 shows that the number of captured G4 biotinylated PAMAM dendrimers tracks with the increase in dendrimer solution concentration. The degree of bound dendrimers was similar for various different areas of the capture surface. A calibration plot of the amount of captured G4 biotinylated PAMAM dendrimers (determined by SPM analysis) as a function of solution concentration is shown in Figure 3(a). The number of captured dendrimers correlates with G4 biotinylated PAMAM dendrimer concentrations, showing a linear dynamic range under the concentrations range evaluated (– μmol/L). This readout method has the potential for low limits of detection. The limit of detection can be estimated as the signal three times above the measurement noise, where the noise is the sample blank response. This corresponds to a limit of detection of ~2.5×10⁻¹³ moles. Results were correlated with a standard HPLC analysis approach for quantification of dendrimers, as shown in Figure 3(b). HPLC quantification of dendrimers shows a linear dynamic range under the concentrations evaluated (–70.35 μmol/L) with a corresponding limit of detection of moles. The capture assay platform improves the limit of detection by a factor of 1000. It should also be noted that the concentrations investigated by the capture assay were not detectable by HPLC analysis.

(a)

(b)

The capture assay platform has shown the potential for low-level detection and quantification of G4 biotinylated PAMAM dendrimers. Further improvements in the performance of this immunosorbent assay approach such as the reduction of incubation times may be possible by utilizing a rotating capture substrate to increase the flux of analyte to the capture surface [38]. In addition, the limit of detection may be further improved by reducing the area dimension of the DSP capture platform. The range of dendrimers that can be quantified using this approach is potentially limited to the analyte capture surface and labeling strategy of the dendrimers. This quantification method can be applied to any type of immunosorbant assay approach (e.g., antibody antigen binding). In addition, the capture platform design could be utilized for multidetection capability. It is important to note, however, that quantification of unfunctionalized dendrimers would require a labeling strategy for this capture assay approach to be used.

The capture assay platform also has the ability to selectively pattern PAMAM dendrimers onto a surface, as shown in Figure 4. In this study a PDMS stamp with a positive structure of 10 μm wide stripes separated by 5 μm stripes was used to pattern G4 biotinylated PAMAM dendrimers using the assay approach. Figures 4(a) and 4(b) show the height and phase analysis of the patterned surface. The bright stripes in the height analysis (Figure 4(a)) correspond to the ODT layer (10 μm wide), and the darker stripe corresponds to the DSP layer (5 μm wide). The height difference (~2.5 nm) is consistent with the differing dimensions of ODT and DSP monolayers. It can be seen from the phase analysis that the captured dendrimers are more easily identifiable in the DSP stripe (Figure 4(b)). Figures 4(c) and 4(d) present higher-resolution height and phase analysis of the patterned G4 biotinylated PAMAM dendrimers. In these SPM images the individual dendrimers bound to the DSP stripe can be ascertained. The dendrimers are individually distributed within the DSP stripe. The dendrimers do not clump together and multilayers of dendrimers are not evident. Furthermore, the ODT layers do not show any evidence of nonspecific adsorption. Cross-sectional height profiles (~4.5 nm) are consistent with G4 dendrimers. The slight variabilities in the height may be due to variations in how the biotin on the dendrimer surface is bound to the avidin capture platform. Further validation of the patterning of the G4 biotinylated PAMAM dendrimers was conducted by tagging the bound dendrimers with Alexa Fluor conjugated avidin, as shown in Figure 5. Fluorescence imaging verifies that the dendrimers are patterned on the avidin capture surface over large surface areas. Analysis of the blank confirms that nonspecific adsorption of G4 biotinylated PAMAM dendrimers is minimal. The bound patterned dendrimers have been found to be stable on the capture platform for >1 year under ambient storage conditions. Although, methods such as direct microcontact printing [42] dip-pen lithography [43], and electron-beam patterning [44] of dendrimers have been reported previously, they do not provide the selective patterning of this approach. The dimensions and profiles of the patterned dendrimers can be modified using different PDMS platforms.

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4. Conclusions

This paper has demonstrated the potential value of immunoimaging SPM to detect and quantify G4 biotinylated PAMAM dendrimers. Results were presented that showed that this new approach using an immunoassay platform provides a 1000-fold improvement in the limit of detection of dendrimers compared to current quantification methods using HPLC. The range of dendrimers that could be evaluated with this approach is potentially limited to the availability of analyte capture and labeling strategies. Findings have also shown the potential of this platform to pattern dendrimers for sensor and nanodevice applications.

Acknowledgments

This project has been funded by the Merck Institute for Science Education, Kentucky NSF EPSCoR, Northern Kentucky University, Center for Integrated Natural Science and Mathematics, and the NKU Research Foundation. This work was also supported by a grant from the Kentucky Biomedical Research Infrastructure Network (P20 RR016481-08).

References

G. M. Dykes, “Dendrimers: a review of their appeal and applications,” Journal of Chemical Technology and Biotechnology, vol. 76, no. 9, pp. 903–918, 2001.
View at: Publisher Site | Google Scholar
D. A. Tomalia, “Birth of a new macromolecular architecture: dendrimers as quantized building blocks for nanoscale synthetic polymer chemistry,” Progress in Polymer Science, vol. 30, no. 3-4, pp. 294–324, 2005.
View at: Publisher Site | Google Scholar
D. A. Tomalia, “The emergence of a new macromolecular architecture: the dendritic state,” in Physical Properties of Polymers Handbook, J. E. Mark, Ed., pp. 671–692, Springer, New York, NY, USA, 2007.
View at: Google Scholar
D. A. Tomalia, S. A. Henderson, and M. S. Diallo, “Dendrimers—an enabling synthetic science to controlled organic nanostructures,” in Handbook of Nanoscience, Engineering and Technology, W. A. I. Goddard, D. W. Brenner, S. E. Lyshevski, and G. J. Irafrate, Eds., pp. 24.1–24.47, CRC Press, Taylor and Francis, Boca Raton, Fla, USA, 2007.
View at: Google Scholar
D. Astruc, E. Boisselier, and C. Ornelas, “Dendrimers designed for functions: from physical, photophysical, and supramolecular properties to applications in sensing, catalysis, molecular electronics, photonics, and nanomedicine,” Chemical Reviews, vol. 110, no. 4, pp. 1857–1959, 2010.
View at: Publisher Site | Google Scholar
V. Gajbhiye, V. K. Palanirajan, R. K. Tekade, and N. K. Jain, “Dendrimers as therapeutic agents: a systematic review,” Journal of Pharmacy and Pharmacology, vol. 61, no. 8, pp. 989–1003, 2009.
View at: Publisher Site | Google Scholar
W. Wijagkanalan, S. Kawakami, and M. Hashida, “Designing dendrimers for drug delivery and imaging: pharmacokinetic considerations,” Pharmaceutical Research, vol. 28, no. 7, pp. 1500–1519, 2011.
View at: Publisher Site | Google Scholar
K. C. Petkar, S. S. Chavhan, S. Agatonovik-Kustrin, and K. K. Sawant, “Nanostructured materials in drug and gene delivery: a review of the state of the art,” Critical Reviews in Therapeutic Drug Carrier Systems, vol. 28, no. 2, pp. 101–164, 2011.
View at: Google Scholar
M. A. Mintzer and M. W. Grinstaff, “Biomedical applications of dendrimers: a tutorial,” Chemical Society Reviews, vol. 40, no. 1, pp. 173–190, 2011.
View at: Publisher Site | Google Scholar
Y. Cheng, L. Zhao, Y. Li, and T. Xu, “Design of biocompatible dendrimers for cancer diagnosis and therapy: current status and future perspectives,” Chemical Society Reviews, vol. 40, no. 5, pp. 2673–2703, 2011.
View at: Publisher Site | Google Scholar
E. Bustos, J. Manríquez, G. Orozco, and L. A. Godínez, “Preparation, characterization, and electrocatalytic activity of surface anchored, Prussian Blue containing starburst PAMAM dendrimers on gold electrodes,” Langmuir, vol. 21, no. 7, pp. 3013–3021, 2005.
View at: Publisher Site | Google Scholar
N. Zhu, Y. Gu, Z. Chang, P. He, and Y. Fang, “PAMAM dendrimers-based DNA biosensors for electrochemical detection of DNA hybridization,” Electroanalysis, vol. 18, no. 21, pp. 2107–2114, 2006.
View at: Publisher Site | Google Scholar
M. S. Diallo, S. Christie, P. Swaminathan, J. H. Johnson Jr., and W. A. Goddard III, “Dendrimer enhanced ultrafiltration—1. Recovery of Cu(II) from aqueous solutions using PAMAM dendrimers with ethylene diamine core and terminal NH 2 groups,” Environmental Science and Technology, vol. 39, no. 5, pp. 1366–1377, 2005.
View at: Publisher Site | Google Scholar
L. J. Twyman, A. S. H. King, and I. K. Martin, “Catalysis inside dendrimers,” Chemical Society Reviews, vol. 31, no. 2, pp. 69–82, 2002.
View at: Publisher Site | Google Scholar
J. N. H. Reek, D. De Groot, G. E. Oosterom, P. C. J. Kamer, and P. W. N. M. Van Leeuwen, “Core and periphery functionalized dendrimers for transition metal catalysis; a covalent and a non-covalent approach,” Reviews in Molecular Biotechnology, vol. 90, no. 3-4, pp. 159–181, 2002.
View at: Publisher Site | Google Scholar
J. Satija, V. V. R. Sai, and S. Mukherji, “Dendrimers in biosensors: concept and applications,” Journal of Materials Chemistry, vol. 21, pp. 14367–14386, 2011.
View at: Google Scholar
J. Losada, M. Zamora, P. García Armada, I. Cuadrado, B. Alonso, and C. M. Casado, “Bienzyme sensors based on novel polymethylferrocenyl dendrimers,” Analytical and Bioanalytical Chemistry, vol. 385, no. 7, pp. 1209–1217, 2006.
View at: Publisher Site | Google Scholar
H. Cavaye, P. E. Shaw, A. R.G. Smith et al., “Solid state dendrimer sensors: effect of dendrimer dimensionality on detection and sequestration of 2,4-dinitrotoluene,” Journal of Physical Chemistry C, vol. 115, no. 37, pp. 18366–18371, 2011.
View at: Publisher Site | Google Scholar
J. Giri, M. S. Diallo, W. A. Goddard, N. F. Dalleska, X. Fang, and Y. Tang, “Partitioning of poly(amidoamine) dendrimers between n-octanol and water,” Environmental Science and Technology, vol. 43, no. 13, pp. 5123–5129, 2009.
View at: Publisher Site | Google Scholar
D. G. Mullen, E. L. Borgmeier, A. M. Desai et al., “Isolation and characterization of dendrimers with precise numbers of functional groups,” Chemistry, vol. 16, no. 35, pp. 10675–10678, 2010.
View at: Publisher Site | Google Scholar
S. Mutalik, A. K. Hewavitharana, P. N. Shaw, Y. G. Anissimov, M. S. Roberts, and H. S. Parekh, “Development and validation of a reversed-phase high-performance liquid chromatographic method for quantification of peptide dendrimers in human skin permeation experiments,” Journal of Chromatography B, vol. 877, no. 29, pp. 3556–3562, 2009.
View at: Publisher Site | Google Scholar
S. Lalwani, V. J. Venditto, A. Chouai, G. E. Rivera, S. Shaunak, and E. E. Simanek, “Electrophoretic behavior of anionic triazine and pamam dendrimers: methods for improving resolution and assessing purity using capillary electrophoresis,” Macromolecules, vol. 42, no. 8, pp. 3152–3161, 2009.
View at: Publisher Site | Google Scholar
M. T. Islam, I. J. Majoros, and J. R. Baker Jr., “HPLC analysis of PAMAM dendrimer based multifunctional devices,” Journal of Chromatography B, vol. 822, no. 1-2, pp. 21–26, 2005.
View at: Publisher Site | Google Scholar
M. T. Islam, X. Shi, L. Balogh, and J. R. Baker, “HPLC separation of different generations of poly(amidoamine) dendrimers modified with various terminal groups,” Analytical Chemistry, vol. 77, no. 7, pp. 2063–2070, 2005.
View at: Publisher Site | Google Scholar
X. Shi, I. Bányai, K. Rodriguez et al., “Electrophoretic mobility and molecular distribution studies of poly(amidoamine)dendrimers of defined charges,” Electrophoresis, vol. 27, no. 9, pp. 1758–1767, 2006.
View at: Publisher Site | Google Scholar
X. Shi, I. Bányai, M. T. Islam et al., “Generational, skeletal and substitutional diversities in generation one poly(amidoamine) dendrimers,” Polymer, vol. 46, no. 9, pp. 3022–3034, 2005.
View at: Publisher Site | Google Scholar
X. Shi, X. Bi, T. R. Ganser et al., “HPLC analysis of functionalized poly(amidoamine) dendrimers and the interaction between a folate-dendrimer conjugate and folate binding protein,” Analyst, vol. 131, no. 7, pp. 842–848, 2006.
View at: Publisher Site | Google Scholar
N. Sato, H. Kobayashi, T. Saga et al., “Tumor targeting and imaging of intraperitoneal tumors by use of antisense oligo-DNA complexed with dendrimers and/or avidin in mice,” Clinical Cancer Research, vol. 7, no. 11, pp. 3606–3612, 2001.
View at: Google Scholar
D. S. Wilbur, P. M. Pathare, D. K. Hamlin, K. R. Buhler, and R. L. Vessella, “Biotin reagents for antibody pretargeting. 3. Synthesis, radioiodination, and evaluation of biotinylated starburst dendrimers,” Bioconjugate Chemistry, vol. 9, no. 6, pp. 813–825, 1998.
View at: Publisher Site | Google Scholar
H. C. Yoon, M. Y. Hong, and H. S. Kim, “Affinity biosensor for avidin using a double functionalized dendrimer monolayer on a gold electrode,” Analytical Biochemistry, vol. 282, no. 1, pp. 121–128, 2000.
View at: Publisher Site | Google Scholar
R. Spector and D. Mock, “Biotin transport through the blood-brain barrier,” Journal of Neurochemistry, vol. 48, no. 2, pp. 400–404, 1987.
View at: Google Scholar
S. Beg, A. Samad, M. I. Alam, and I. Nazish, “Dendrimers as novel systems for delivery of neuropharmaceuticals to the brain,” CNS and Neurological Disorders, vol. 10, no. 5, pp. 576–588, 2011.
View at: Google Scholar
N. L. Rosi and C. A. Mirkin, “Nanostructures in biodiagnostics,” Chemical Reviews, vol. 105, no. 4, pp. 1547–1562, 2005.
View at: Publisher Site | Google Scholar
B. Basnar and I. Willner, “Dip-pen-nanolithographic patterning of metallic, semiconductor, and metal oxide nanostructures on surfaces,” Small, vol. 5, no. 1, pp. 28–44, 2009.
View at: Publisher Site | Google Scholar
A. N. Shipway, E. Katz, and I. Willner, “Nanoparticle arrays on surfaces for electronic, optical, and sensor applications,” ChemPhysChem, vol. 1, no. 1, pp. 18–52, 2000.
View at: Google Scholar
C. A. Cason, S. A. Oehrle, T. A. Fabre et al., “Improved methodology for monitoring poly(amidoamine) dendrimers surface transformations and product quality by ultra performance liquid chromatography,” Journal of Nanomaterials, vol. 2008, Article ID 456082, 7 pages, 2008.
View at: Publisher Site | Google Scholar
J. D. Driskell, K. M. Kwarta, R. J. Lipert, M. D. Porter, J. D. Neill, and J. F. Ridpath, “Low-level detection of viral pathogens by a surface-enhanced Raman scattering based immunoassay,” Analytical Chemistry, vol. 77, no. 19, pp. 6147–6154, 2005.
View at: Publisher Site | Google Scholar
J. D. Driskell, J. M. Uhlenkamp, R. J. Lipert, and M. D. Porter, “Surface-enhanced Raman scattering immunoassays using a rotated capture substrate,” Analytical Chemistry, vol. 79, no. 11, pp. 4141–4148, 2007.
View at: Publisher Site | Google Scholar
R. L. Millen, J. Nordling, H. A. Bullen, M. D. Porter, M. Tondra, and M. C. Granger, “Giant magenetoresistive sensors. 2. Detection of biorecognition events at self-referencing and magnetically tagged arrays,” Analytical Chemistry, vol. 80, no. 21, pp. 7940–7946, 2008.
View at: Publisher Site | Google Scholar
D. E. Q. Yang, Y. U. Q. Xiong, Y. Guo, D. A. Da, and W. G. Lu, “Sizes correction on AFM images of nanometer spherical particles,” Journal of Materials Science, vol. 36, no. 1, pp. 263–267, 2001.
View at: Publisher Site | Google Scholar
P. Markiewicz and M. C. Goh, “Simulation of atomic force microscope tip-sample/sample-tip reconstruction,” Journal of Vacuum Science and Technology B, vol. 13, no. 3, pp. 1115–1118, 1995.
View at: Publisher Site | Google Scholar
X. C. Wu, A. M. Bittner, and K. Kern, “Microcontact printing of CDS/dendrimer nanocomposite patterns on silicon wafers,” Advanced Materials, vol. 16, no. 5, pp. 413–417, 2004.
View at: Google Scholar
R. McKendry, W. T. S. Huck, B. Weeks, M. Fiorini, C. Abell, and T. Rayment, “Creating nanoscale patterns of dendrimers on silicon surfaces with dip-pen nanolithography,” Nano Letters, vol. 2, no. 7, pp. 713–716, 2002.
View at: Publisher Site | Google Scholar
P. Bhatnagar, S. S. Mark, I. Kim et al., “Dendrimer-Scaffold-based electron-beam patterning of biomolecules,” Advanced Materials, vol. 18, no. 3, pp. 315–319, 2006.
View at: Publisher Site | Google Scholar

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Copyright © 2012 Chevelle A. Cason et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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