Self-assembled Multilayer Films Research Articles

Real-Time Cell Temperature Fluctuation Monitoring System Using Precision Pt Sensors Coated with Low Thermal Capacity, Low Thermal Resistance, and Self-Assembled Multilayer Films.

Real-time monitoring of cell temperature fluctuation can help researchers better understand physiological phenomena and the effects of drug treatment on cells, which is a novel and important tool for cellular informatics. The platinum (Pt) temperature sensor is widely used in temperature measurement with the advantages of strong stability, great accuracy, and high sensitivity. However, the commercially available Pt sensors have large thermal resistance and heat capacity which are difficult to be applied for cell temperature measurement because only a very small amount of heat flux is generated by live cells. In this study, we designed a system using precision Pt thin-film temperature sensors with low heat capacity and thermal resistance. The Pt thin-film sensors are covered by a silicon nitride insulation layer grafted with a self-assembled multilayer silane film for promoting cell adhesion. The temperature coefficient of resistance of the Pt temperature sensor was about 2100 ppm/°C. The four-wire lead design next to the sensor detection area ensured maximum accuracy, resulting in a system noise below 0.01 °C over a long time. HEK-293T and HeLa cells were cultured on the sensor surface, respectively. The temperature fluctuation of 293T cells was monitored in a cell culture medium, showing a temperature increase of about 0.05-0.12 °C. The temperature fluctuation of HeLa cells treated with cisplatin was also measured and recorded, indicating a temperature decrease of 0.01 °C first and then a gradual temperature increase of 0.04 °C. The Pt sensor system we developed demonstrated high sensitivity and long stability for cell temperature fluctuation monitoring, which can be widely used in cell activity and cellular informatics studies.

Fluorescence Signal Enhancement by a Spray-Assisted Layer-by-Layer Technique on Aluminum Tape Devices for Biosensing Applications

Layer-by-layer (LbL) self-assembled polyelectrolyte multilayer (PEM) films are a simple yet elegant bottom-up technology to create films at the nano-microscale. This low-cost technology has been widely used as a universal functionalization technique on a broad spectrum of substrates. Biomolecules under investigation can be incubated onto films based on complementary charge interactions between the films and biomolecules. There is a great demand for developing an ultralow-cost biosensing device, which can optimally enhance the fluorescence signal of the adsorbed biomolecules from the traditional labeled sensing platforms. In this work, we have incorporated a blend of the conventional metal enhanced fluorescence technology and the PEM as a dielectric spacer and functionalized film, coated on an aluminum paper (tape)-based substrate. These device has been found to be capable of holding biomolecules in three-dimensional PEM space. The devices fabricated by the proposed spray LbL technique provide significant fluorescence signal enhancement by holding a relatively higher mass per volume of the adsorbed biomolecules, when compared to traditional spin- and dip-coating techniques. Interestingly, our proposed device has expressed a fluorescence enhancement factor, which is 9 times higher than PEM-functionalized glass-based devices. To demonstrate the practical utility of our devices, we also compared our devices to Whatman FAST slides. Our experimental fluorescence results are almost comparable to Whatman FAST slides. Such PEM devices fabricated on top of low-cost aluminum tape using a spray LbL technique give new insights into the future development of ultralow-cost, high-throughput, and disposable lab-on-chip diagnostic applications.

High Loading Capacity and Wear Resistance of Graphene Oxide/Organic Molecule Assembled Multilayer Film.

Taking advantage of the strong charge interactions between negatively charged graphene oxide (GO) sheets and positively charged poly(diallyldimethylammonium chloride) (PDDA), self-assembled multilayer films of (GO/PDDA)n were created on hydroxylated silicon substrates by alternating electrostatic adsorption of GO and PDDA. The formation and structure of the films were analyzed by means of water contact angle measurement, thickness measurement, atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). Meanwhile, tribological behaviors in micro- and macro- scale were investigated by AFM and a ball-on-plate tribometer, respectively. The results showed that (GO/PDDA)n multilayer films exhibited excellent friction-reducing and anti-wear abilities in both micro- and macro-scale, which was ascribed to the special structure in (GO/PDDA)n multilayer films, namely, a well-stacked GO–GO layered structure and an elastic 3D crystal stack in whole. Such a film structure is suitable for design molecular lubricants for MEMS and other microdevices.

Construction of a Self-Assembled Polyelectrolyte/Graphene Oxide Multilayer Film and Its Interaction with Metal Ions.

In this study, a composite multilayer film onto gold was constructed from two charged building blocks, i.e., negatively charged graphene oxide (GO) and a branched polycation (polyethylenimine, PEI) via layer-by-layer (LbL) self-assembly technology, and this process was monitored in situ with quartz crystal microbalance (QCM) under different experimental conditions. This included the differences in frequency (Δf) as well as the changes in dissipation to yield information on the absorbed mass and viscoelastic properties of the formed PEI/GO multilayer films. The experimental conditions were optimized to obtain a high amount of the adsorbed mass of the self-assembled multilayer film. The surface morphology of the PEI/GO multilayer film onto gold was studied with atomic force microscopy (AFM). It was found that the positively charged PEI chains were combined with the oppositely charged GO to form an assembled film on the QCM sensor surface, in a wrapped and curled fashion. Raman and UV-vis spectra also showed that the intensities of the GO-characteristic signals are almost linearly related to the layer number. To explore the films for their use in divalent ion detection, the frequency response of the PEI/GO multilayer-modified QCM sensor to the exposure of aqueous solutions solution of Cu2+, Ca2+, Zn2+, and Sn2+ was further studied using QCM. Based on the Sauerbrey equation and the weight of different ions, the number of metal ions adsorbed per unit area on the surface of QCM sensors was calculated. For metal ion concentrations of 40 ppm, the adsorption capacities per unit area of Cu2+, Zn2+, Sn2+, and Ca2+ were found to be 1.7, 3.2, 0.7, and 4.9 nmol/cm2, respectively. Thus, in terms of the number of adsorbed ions per unit area, the QCM sensor modified by PEI/GO multilayer film shows the largest adsorption capacity of Ca2+. This can be rationalized by the relative hydration energies.

Ultrafast third order nonlinear optical properties of self-assembled indium phthalocyanine multilayer films

An ultrathin composite films with alternated layers containing anionic lithium tetracarboxyl indium phthalocyanine chloride (ClInPc(COOLi)4) and cationic poly(diallydimethyl ammonium chloride) (PDDA) were prepared using layer-by-layer assembly technique. The resulting films were characterized by Ultraviolet-visible and Fourier transform infrared spectroscopy, showing regularly consecutive adsorption. The ultrafast third-order nonlinear optical properties of the films were investigated via a 4f coherent imaging system with phase object with 190 fs laser pulses at 532nm. The results demonstrate that the ultrathin films exhibited excellent self-focusing effect (n2 ∼ 8.86 × 10−17 m2/W) and reverse saturable absorption properties (β ∼ 5.19 × 10−10 m/W), while the nonlinear optical response of the same composite in aqueous solution were found to be negligible. Our results indicate that the ClInPc(COOLi)4/PDDA film is a promising candidate for future nonlinear optical devices.

A highly conductive self-assembled multilayer graphene nanosheet film for electronic tattoos in the applications of human electrophysiology and strain sensing.

Highly conductive, conformable and gel-free electrodes are desirable in human electrophysiology. Besides, intimately coupling with human skin, wearable strain sensors can detect numerous physiological signals, such as wrist pulse and breath. In this study, a multilayer graphene nanosheet film (MGNF) with high conductivity was prepared by the Marangoni self-assembly for using in tattoo dry electrodes (TDEs) and in a graphene tattoo strain sensor (GTSS). Compared to commercial Ag/AgCl gel electrodes, TDEs have lower skin-electrode contact impedance and could detect human electrocardiogram for 24-hour wearing more accurately as well as electromyogram. Through designing a slim serpentine ribbon structure, a resistance-type GTSS, without deterioration even after 2000 cycles, is well demonstrated for human wrist pulse and breath sensing. With the advantages of high conductivity and conformability, MGNF provides support to fabricate low-cost, customizable, and high-performance electronic tattoos for human electrophysiology and strain sensing.

A smart and active film with tunable drug release and color change abilities for detection and inhibition of bacterial growth.

Antimicrobial resistance has become a global issue and thus the development of natural products/biomedical materials composites with antibacterial activities is urgently needed. When acute wounds develop into chronic wounds, the wound environments become alkaline. As long as infections occur, the wound pH further increases, making the wounds difficult to heal. Besides, bacterial growth in poultry, meat, fish and seafood products is usually reflected in a marked increase of pH values. Herein, smart, stimuli responsive self-assembled multilayer and complex film were constructed through the formation of hydrogen bonds and hydrophobic interactions between hydroxypropyl methylcellulose (HPMC) and epigallocatechin-3-gallate (EGCG), thereby greatly reducing the hydrophilicity of HPMC and offering enhanced mechanical strength, superior free radical scavenging capability, and improved water vapor and light barrier properties. The EGCG/HPMC complex film was able to control EGCG release by tuning pH or temperature of the release medium. Furthermore, incorporation of CuS nanoparticles into the film allowed it to triggers EGCG release in an on-demand fashion under near-infrared (NIR) exposure. Bacterial growth in glucose-free nutrient broth medium caused pH to rise (near pH8.0), leading to transformation of EGCG from phenol type to phenolate ion and then quinone, allowing for spontaneous generation of H2O2 to kill bacteria. The complex films changed their color in response to bacterial growth because EGCG transformed from phenol type to quinone type under alkaline condition. The green synthesized EGCG/HPMC complex films can be used as a colorimetric pH indicator and an antibacterial material for wound dressing and food packaging applications.

Layer-by-layer self-assembled multilayer films of sulfonated-β-cyclodextrin and its reversible adsorption of methyl orange

Multilayer film based on photosensitive p-diphenyl diazonium salt (biPh-N2+) and sulfonated-β-cyclodextrin (S-β-CD) were fabricated by layer-by-layer self-assembly. The ionic bonds formed between diazonium salt and sulfonic acid ion in the multilayer film converted to covalent bonds and formed stable ultra-thin film when the diazonium groups decomposed under UV light irradiation. Meanwhile, the concentration of S-β-CD aqueous solution can influence the self-assembled multilayer films, while the pH value (pH=3~9) had little effect on the self-assembled process except the strong alkaline solution (pH=11). Moreover, based on the electrostatic interactions of S-β-CD and MO to form a host-guest complexation, the multilayer film of (biPh-N2+/S-β-CD)12 can absorb methyl orange (MO), and which can release reversibly in ethanol.

PH-responsive and antibacterial properties of self-assembled multilayer films based on chitosan and tannic acid.

Polyelectrolyte layer-by-layer (LbL) films that disintegrate under physiological conditions are intensively studied as coatings to enable the release of bioactive components. Herein, we report on the interactions and pH-stability of LbL films composed of chitosan (CH) or N-(2-hydroxypropyl)-3-trimethylammonium chitosan chloride (CMCH) and tannic acid (TA), employed to guarantee the film disintegration. The self-assembly of TA with CH and CMCH at pH5 and with CMCH at pH7.4 were proven by turbidimetric, surface plasmon resonance and UV-Vis analyses. The LbL films exhibited pH-dependent properties; CMCH/TA films prepared at pH7.4 showed exponential growth as well as a higher layer thickness and surface roughness, whereas films prepared at pH5 grew linearly and were smoother. The film stability varied with the pH used for film assembly; CH/TA films assembled at pH5 were unstable at pH8.5, whereas CMCH/TA films assembled at pH7.4 disintegrated at pH4. All films exhibited a similar disassembly at pH7.4. The coatings reduced the adhesion of E. coli and S. aureus by approximately 80%. CMCH-terminated CMCH/TA films were more resistant to bacterial adhesion, whereas CH-terminated CH/TA films demonstrated stronger killing activity. The prepared pH-triggered decomposable LbL films could be used as degradable coatings that allow the release of therapeutics for biomedical applications and also prevent bacterial adhesion.

Self-Assembled Multilayer Films for Time-Controlled Ocular Drug Delivery.

The patient's compliance on the therapeutics to treat glaucoma is significantly low contributing for a fast evolution of the disease. This article presents an autonomous system with controlled release using an alpha2-adrenergic receptor agonist, brimonidine, usually used to treat glaucoma. More specifically, biocompatible and layer-by-layer drug delivery films containing monolayers with brimonidine encapsulated in polymer-β-cyclodextrin were prepared with the objective to obtain a system able to release precise amounts of drug at specific times. To delay the erosion-controlled drug release, we included nanosheets of graphene oxide and layers of a biodegradable polymer (poly-β-aminoester) between the drug-containing monolayers to obtain a time-controlled drug delivery system. An increase in the number of graphene oxide layers is proportional to the brimonidine release delay and its kinetic release can be tuned as a function of the number of layers. Two types of films with brimonidine encapsulated in β-cyclodextrin were analyzed. One of them composed of barrier layers with PBAE and another with two types of barrier layers, PBAE and graphene oxide. The results indicate that one graphene oxide bilayer can delay the brimonidine release for more than 24 h. In vitro assays confirmed that the films have a cell viability of 100%.

Dynamic Self-Assembly of Polyelectrolyte Composite Nanomaterial Film.

The aim of this study is not only to investigate the feasibility of using PAH (polyallylamine hydrochloride) and PSS (poly styrene-4-sulfonic acid sodium salt) to prepare a film via a layer by layer self-assembly process entrained with silver nanoparticles, but also to show that the silver nanoparticles crystalline structure can be defined and deposited on the surface of the substrate in the desired alignment structure and manner, which is of great help to research on the LBL method in the cellulose field. The effect of outermost layer variation, assembly layers, and composition of multilayers on the formation of the LBL structure on a nanofibrillated cellulose (NFC)/polyvinyl alcohol (PVA) substrate was investigated. The deposition of PAH and PSS was monitored by Fourier-transform infrared spectroscopy (FT-IR). The morphology of the LBL film layers was observed by scanning electron microscope (SEM) and atomic force microscope (AFM). Furthermore, thermal degradation properties were investigated by thermogravimetric analysis (TGA), and physical properties of multilayer films were tested by a universal mechanical tester. The results reveal that PAH and PSS can be readily deposited on a NFC/PVA substrate by using LBL methodology to prepare self-assembled polyelectrolyte multilayer films. The surface morphology of the LBL composite changed from negative to positive charged depending on the final LBL treatment. Also, according to SEM and AFM analysis, silver nanoparticles were well dispersed in the (PAH/PSS) film, which significantly improved the thermal stability of the composite films.

The Application of a Nanomaterial Optical Fiber Biosensor Assay for Identification of Brucella Nomenspecies.

Bacteria in the genus Brucella are the cause of brucellosis in humans and many domestic and wild animals. A rapid and culture-free detection assay to detect Brucella in clinical samples would be highly valuable. Nanomaterial optical fiber biosensors (NOFS) are capable of recognizing DNA hybridization events or other analyte interactions with high specificity and sensitivity. Therefore, a NOFS assay was developed to detect Brucella DNA from cultures and in tissue samples from infected mice. An ionic self-assembled multilayer (ISAM) film was coupled to a long-period grating optical fiber, and a nucleotide probe complementary to the Brucella IS711 region and modified with biotin was bound to the ISAM by covalent conjugation. When the ISAM/probe duplex was exposed to lysate containing ≥100 killed cells of Brucella, or liver or spleen tissue extracts from Brucella-infected mice, substantial attenuation of light transmission occurred, whereas exposure of the complexed fiber to non-Brucella gram-negative bacteria or control tissue samples resulted in negligible attenuation of light transmission. Oligonucleotide probes specific for B. abortus, B. melitensis, and B. suis could also be used to detect and differentiate these three nomenspecies. In summary, the NOFS biosensor assay detected three nomenspecies of Brucella without the use of polymerase chain reaction within 30 min and could specifically detect low numbers of this bacterium in clinical samples.

Fabrication of Supramolecular Bioactive Surfaces via β-Cyclodextrin-Based Host-Guest Interactions.

Supramolecular host-guest interactions provide a facile and versatile basis for the construction of sophisticated structures and functional assemblies through specific molecular recognition of host and guest molecules to form inclusion complexes. In recent years, these interactions have been exploited as a means of attaching bioactive molecules and polymers to solid substrates for the fabrication of bioactive surfaces. Using a common host molecule, β-cyclodextrin (β-CD), and various guest molecules as molecular building blocks, we fabricated several types of bioactive surfaces with multifunctionality and/or function switchability via host-guest interactions. Other groups have also taken this approach, and several intelligent designs have been developed. The results of these investigations indicate that, compared to the more common covalent bonding-based methods for attachment of bioactive ligands, host-guest based methods are simple, more broadly ("universally") applicable, and allow convenient renewal of bioactivity. In this Spotlight on Applications, we review and summarize recent developments in the fabrication of supramolecular bioactive surfaces via β-CD-based host-guest interactions. The main focus is on the work from our laboratory, but highlights on work from other groups are included. Applications of the materials are also emphasized. These surfaces can be categorized into three types based on: (i) self-assembled monolayers, (ii) polymer brushes, and (iii) multilayered films. The host-guest strategy can be extended from material surfaces to living cell surfaces, and work along these lines is also reviewed. Finally, a brief perspective on the developments of supramolecular bioactive surfaces in the future is presented.

Identification of Histophilus somni by a nanomaterial optical fiber biosensor assay.

Histophilus somni is an opportunistic pathogen responsible for respiratory and systemic diseases of cattle and sheep. Rapid and accurate detection of H. somni is essential to distinguish H. somni from other potential pathogens for proper control and treatment of infections. Nanomaterial optical fiber biosensors (NOFS) recognize analyte interactions, such as DNA hybridization, with high specificity and sensitivity, and were applied to detect H. somni DNA in culture and clinical samples. An ionic self-assembled multilayer (ISAM) film was fabricated on a long-period grating optical fiber, and a biotinylated, nucleotide probe complementary to the H. somni 16S rDNA gene was coupled to the ISAM film. Exposure of the ISAM::probe to ⩾100 killed cells of H. somni strain 2336 without DNA amplification resulted in attenuation of light transmission of ⩾9.4%. Exposure of the complexed fiber to Escherichia coli or non- H. somni species of Pasteurellaceae reduced light transmission by ⩽3.4%. Exposure of the ISAM::probe to blood, bronchoalveolar fluid, or spleen from mice or calves infected with H. somni resulted in ⩾24.3% transmission attenuation. The assay correctly detected all 6 strains of H. somni tested from culture, or tissues from 3 separate mice and calves tested in duplicate. Six heterologous strains (representing 6 genera) reacted at below the cutoff value of 4.87% attenuation of light transmission. NOFS detected at least 100 H. somni cells without DNA amplification within 45 min with high specificity. Although different fibers could vary in signal sensitivity, this did not affect the sensitivity or specificity of the assay.

Poly-l-lysine/poly-l-glutamic acid-based layer-by-layer self-assembled multilayer film for nitric oxide gas delivery

Nitric oxide (NO) gas is an endogenously produced radical gas involved in numerous physiological and pathological processes in the human body and shows potential for biomedical applications. Numerous studies have attempted to develop an NO-releasing platform in the past few decades. To take advantage of exogenous NO gas delivery, controlling the total concentration and release profile are the most important factors. To develop a controlled NO-releasing system, we used the poly-l-lysine (PLL) and poly-l-glutamic acid (PGA) because of their high biocompatibility in biomedical applications. We constructed (PLL/PGA)n multilayer thin films using the layer-by-layer self-assembly technique. We then synthesized the N-diazeniumdiolate, a proton-responsive NO donor, into the polypeptide multilayer film in a high-pressure reaction under NO gas. We investigated the film growth profile by quartz crystal microbalance and thickness measurements and determined the film surface morphology by scanning electron microscopy and atomic force microscopy. By comparing films with different thicknesses, we confirmed NO donor formation by UV–vis and Fourier-transform infrared spectroscopy. We also determined the release profiles of each film using a real-time NO analysis machine (NOA280i).

Sensitive detection of fractalkine based on AuNPs and metal-organic frameworks composite at para-sulfonatocalix[4]arene-AuNPs assembled multilayer interface

Fractalkine (FKN) has been claimed as a predictive biomarker of Barrett's Esophagus for the first time recently, whereas there are few methods for quantitative detection of FKN. In order to develop a sensitively electrochemical biosensor of FKN, pSC4-AuNPs self-assembled multilayer film on the gold electrode surface was utilized to immobilize anti-FKN as a biorecognition surface. A novel porous para-sulfonatocalix[4]arene-coated gold nanoparticles-functionalized metal-organic frameworks (pSC4-AuNPs/Cu-MOFs) was fabricated to recognize FKN by FKN aptamer and as signal tags for H2O2 catalysis. pSC4-AuNPs multilayer displayed good biocompatibility and high electronic transmission. Combing with the good catalysis ability of Cu-MOFs, the quantitative FKN detection was achieved by the sensitive electrochemical immunosensor with the detection limit of 7.4 pg/mL. With this design, the signal amplification strategy of the pSC4-AuNPs/Cu-MOFs composite offers a potential application of clinical detection of FKN.

CHARACTERIZATION OF OCTADECYLTRICHLOROSILANE SELF-ASSEMBLED MULTILAYERS ON PYREX GLASS

In this paper, octadecyltrichlorosilane (OTS) self-assembled multilayer (SAM) films are fabricated on Pyrex glass by dipping method. The hydrophobicity, constituent and surface morphology of OTS SAM at various dipping times in solutions of 1, 2 and 5[Formula: see text]mM concentrations are investigated. Characteristic absorption peaks around 2850 and 2920[Formula: see text]cm[Formula: see text] are observed by FTIR and island-like structures on samples are detected by AFM. After 15[Formula: see text]min dipping time for solution of 5[Formula: see text]mM, water contact angle of the sample reaches the maximum value of 116.4[Formula: see text] with relatively low surface root mean square (Rms) roughness of 0.152[Formula: see text]nm. The critical surface tension ([Formula: see text] of the analyzed sample is 18.2[Formula: see text]dyne/cm. The optimum dipping time in the solution of 5[Formula: see text]mM for a complete SAM film is about 30[Formula: see text]min. The study of the optimal conditions for the formation of integrated OTS SAM has significant scientific and practical values in modification of solid surfaces.

Use of Modified Colloids and Membranes to Remove Metal Ions from Contaminated Solutions

An efficient process was developed allowing the removal of metal ions from polycontaminated aqueous solutions by combining modified colloids and membranes. Firstly, filtration experiments were performed using polyethersulfone membranes modified by a self-assembled multilayer film of polyelectrolytes. These polymer-modified membranes allowed the uptake of more than 90% of the metal ions initially present in the contaminated solutions (for solutions concentrated at 50 mg L−1). Secondly, adsorption experiments were carried out with colloidal silica encapsulated with carboxymethyl chitosan (SiO2-CMCS) or with mesoporous silica functionalized by grafting of 1,4,8,11-tetraazacyclotetradecane, i.e., cyclam (SiO2-cyclam). The adsorption capacity of these compounds was shown to be higher than numerous other literature-known adsorbents, reaching 68 and 61 mg g−1 towards Cu(II) for SiO2-CMCS and SiO2-cyclam, respectively. Finally, by coupling adsorption with ultrafiltration in the tangential mode, the removal of Cu(II), Ni(II) and Zn(II) ions was found to be improved, allowing to reach a removal efficiency of 99% towards Cu(II), Ni(II) and Zn(II) ions at a metal concentration of 50 mg L−1, and a promising removal efficiency around 70% at a very high metal concentration of 1200 mg L−1. The mechanisms involved in the capture of the metal ions by modified membranes and colloids are also discussed.

Optical nonlinearities and excited state dynamics of self-assembled cobalt phthalocyanine multilayer films

An ultrathin composite films containing cobalt phthalocyanine (CoPc) and poly(diallydimethyl ammonium chloride) (PDDA) were fabricated through layer-by-layer assembly technique. The resulting films were characterized by UV-Vis spectroscopy and atomic force microscopy. Their third-order nonlinear optical properties and photo-excitation dynamics were investigated with 20 ps laser pulses at 532 nm. The results demonstrate that the ultrathin films have notable third order optical nonlinearities (χ(3)∼4.7 × 10−9 (esu)) and fast excited-state relaxation (τ∼67 ± 6 ps), indicating their potential applications in future nonlinear optical devices.

Surface Physicochemical and Structural Analysis of Functionalized Titanium Dioxide Films

Titanium and its alloys are recognized as acceptable materials for many applications. The properties of titanium dioxide (TiO2) thin films are directly related to the structural characteristics of the material, which can be modified with tailor-made functional groups. Reactive bifunctional groups can be bound with hydroxyl-terminated TiO2, leading to the formation of self-assembled monolayers or multilayer films. The understanding of such interactions is necessary to design functional oxide coatings for a large variety of applications. In this study, nanosized TiO2 films were synthesized by the sol-gel method and deposited by spin coating technique upon titanium substrate. Subsequently, TiO2 thin films were functionalized with (3-aminopropyl)trimethoxysilane (APTMS), 3-(4-aminophenyl)propionic acid (APPA), 3-mercaptopropionic acid (MPA) or polyethylene glycol (PEG). Surface characterization by XPS, surface roughness, and contact angle indicated successful functionalization and allowed for identification of the preferential conformation of each molecule. APPA and APTMS presented free amine groups indicating the attachment to the surface by carboxyl and silane groups, respectively. Mercapto coupling from MPA showed the formation of S-Ti bonds. PEG-coated surface revealed polymerization of several hydroxyl groups that crosslinked with each other. Analyzing the mode of attachment at the interface of the metal oxide and functional group may help in the development of improved functional materials.