Keypad Lock Research Articles

Implementation of Digital Computing by Colloidal Crystal Engineering with DNA.

Toehold-mediated strand displacement (TMSD) provides a versatile toolbox for developing DNA digital computing systems. Although different logic circuits with diverse functions have achieved good performance in terms of complexity and scalability, most previous DNA logic circuits perform information processing only at the molecular level, and nonspecific signal leakages are often difficult to avoid. Here, we demonstrate the feasibility of constructing leakless digital computing systems in three-dimensionally ordered colloidal supercrystals. These systems possess a unique signal leakage resistance by integrating different TMSD-based logic gates with the catalytic assembly of DNA-functionalized gold colloids. A complete set of basic Boolean logic gates and different cascaded logic circuits is constructed on the basis of the catalytic assembly strategy enabled by a facilely designed catassembler, where the output signals are recognized by determining whether specific colloidal supercrystals are formed or not. In addition, a half adder is built through a combination of XOR and AND logic gates with two distinct crystal types as readouts. Finally, a leakless two-digit DNA keypad lock for information security protection is demonstrated. The combination of TMSD-based logic circuits with the universal nanoparticle catalytic assembly offers the possibility to develop highly complicated and leakage-free digital computing systems and promotes macroscopic colloidal superlattice materials with programmable logic functions.

Sequential-dependent synthesis of gold-chromium nanocomposites for multimode colorimetric sensing, advanced logic computing, and tri-layer information protection

Binary materials combine the properties and advantages of their components, but their fabrication paradigm needs updating to fully exploit their characteristics and broaden their application. Here, multifunctional bimetallic gold-chromium nanocomposites (Au–Cr NCs) were synthesized facilely in a sequential-dependent manner, and applied from multi-channel sensing to molecular informatization (including advanced logic computing and tri-layer information protection). By sequentially mixing Cr6+, Au3+, and NaBH4 (reducing agent), Au–Cr NCs with Au nanoparticles attached to Cr nanobelts can be prepared easily and quickly. The resulting Au–Cr NCs exhibited multi-signal sensing capability for hypochlorite, with significantly improved selectivity (about 5 times) and sensitivity (about 1650 times) when analyzing multiple signals. The synthesis process can be used to implement parallel molecular logic gates and customizable keypad lock operations. Moreover, by digitizing logical relationships and multimodal selective responses based on Au–Cr NCs, specific information (wise sayings and literary works sentence) can be encoded, encrypted and hidden to realize nano-cryptography and steganography. When combined with molecular keypad lock, a tri-layer information protection system can be constructed to enhance anti-cracking ability. This study promotes controllable preparation and multi-purpose applications of advanced multifunctional nanocomposites, but also opens up a new direction for nano-based sensing and digitization in multi-dimension.

Design and development of an azo dye‐based ultra‐sensitive chemosensor for the ubiquitous organic anion in aqueous solutions

AbstractOxalate plays a crucial role in various biological and industrial applications. Its involvement in diseases, drug‐ and toxin‐induced disorders, and disruption of industrial processes makes it a high‐priority chemical for the development of more precise, selective, and straightforward analytical methods. Herein, an innovative and efficient strategy for sequentially measuring Cu2+ and oxalate ions is reported. During an indicator displacement process, where Cu2+ and azo dye, ArsenazoIII (AAIII), are used as receiver and indicator, respectively, oxalate (C2O42−) is measured by a colorimetric method. Proof of concept results from UV–visible spectroscopy, naked eye, and signal reset of the indicator revealed a more robust interaction of the Cu2+ receptor with C2O42− than the AAIII indicator with high selectivity, good sensitivity, and lower detection limit(4.01 × 10−8 and 3.04 × 10−9mol L−1, for Cu2+ and C2O42−, respectively). The results of measuring C2O42− in actual samples (urine, mushrooms, and spinach) showed the applicability of the existing method. Most importantly, the colorimetric system based on molecular exchange in the indicator dislocation proceeding can serve as a colorimetric INHIBIT logic‐gate. It works like a molecular keypad lock system that can be controlled by two users with two different sets of chemical passwords (inputs) that can be identified through optical paths.

Enhancing Control Over Nitric Oxide Photorelease via a Molecular Keypad Lock.

Based on Boolean logic, molecular keypad locks secure molecular information, typically with an optical output. Here we investigate a rare example of a molecular keypad lock with a chemical output. To this end, the light-activated release of biologically important nitric oxide from a ruthenium complex is studied, using proton concentration and photon flux as inputs. In a pH-dependent equilibrium, a nitritoruthenium(II) complex is turned into a nitrosylruthenium(II) complex, which releases nitric oxide under irradiation with visible light. The precise prediction of the output nitric oxide concentration as function of the pH and photon flux is achieved with an artificial intelligence approach, namely the adaptive neuro-fuzzy inference system. In this manner an exceptionally high level of control over the output concentration is obtained. Moreover, the provided concept to lock a chemical output as well as the output prediction may be applied to other (photo)release schemes.

Dual function Schiff-base as a selective fluorescence “Turn-on” sensor for Zn2+ and a colorimetric sensor for Cu2+ and Fe3+ ions

A simple and adaptable salen-based Schiff base receptor (L = 6,6′-((1E,1′E)-(cyclohexane-1,2-diylbis(azanylylidene))bis(methanylylidene))bis(2-methoxyphenol))was employed in the current study for colorimetric detection of Cu2+, Fe3+, and fluorescence detection of Zn2+ ions in a semi-aqueous solution. L could identify the three target ions among the many different cations and anions in the solution. The turn-on fluorescence signal of L to Zn2+ ions was boosted by the restriction of the intramolecular charge transfer process, and the resulting chelation enhances the fluorescence signal. The sensing mechanisms were validated using a Job’s plot, Electrospray Ionization Mass Spectrometry (ESI-MS) analysis, Nuclear Magnetic Resonance (NMR) titration experiment, and theoretical calculation investigations. The detection limits for Zn2+ were determined to be 0.038 μM, whereas Cu2+ and Fe3+ detection limits were 0.58 μM and 0.62 μM, respectively. Next, L was used to develop solid silica gel and test strips for instantaneous colorimetric and fluorescent detection of the three target ions in real time. The trace level of Cu2+ and Fe3+ in the tap and drinking water samples could be quantitatively measured using L. Eventually, applications for keypad locks and molecular logic gates were developed utilizing the receptor L.

A simple, sensitive, and selective colorimetric chemosensor for sequential determination of dual analytes, Ce3+, H2PO4−, and its applications in the logic gate construction and the system of keypad lock

AbstractSodium (E)‐3‐hydroxy‐4‐((2‐hydroxynaphthalen‐1‐yl)diazenyl)naphthalene‐1‐sulfonate (Calcon, CAL), is employed for the first time as a reversible colorimetric chemosensor to detect and measure Ce3+ and H2PO4− sequentially in the aqueous medium. The detection process has two steps. The interaction of CAL and Ce3+ in the first step with a noticeable color shift from purple to blue. Further, the reaction between CAL‐Ce3+ and H2PO4− shows a clear color return from blue back to initial purple similar to that for CAL. The UV–visible examination of this color return reveals that H2PO4− removes Ce3+ and restores CAL content. The results showed that CAL and CAL‐Ce3+ had a strong binding affinity and adequate detection limits for the Ce3+ and H2PO4−, respectively. For Ce3+, the linear range and detection limit are 1.20 × 10−6‐1.02 × 10−4 and 2.0 × 10−7molL−1, while for H2PO4−, they are 2.0 × 10−7‐8.7 × 10−6 and 3.0 × 10−8 molL−1. Finally, we measured these two ions in real samples using this methodology. Furthermore, the examination of the suggested receptor's logical behavior revealed that it can operate as a colorimetric chemosensor of the INHIBIT type, receiving chemical inputs and producing a UV–visible absorbance signal as the output. If Ce3+ and H2PO4− inputs are added in proper order, the receptor may also function as a molecular “keypad lock.”

Photocleavable DNA Nanotube-Based Dual-Amplified Resonance Rayleigh Scattering System for MicroRNA Detection Incorporating Molecular Computing-Cascaded Keypad Lock Functionality.

Cascade molecular events in complex systems are of vital importance for enhancing molecular diagnosis and information processing. However, the conversion of a cascaded biosensing system into a multilayer encrypted molecular keypad lock remains a significant challenge in the development of molecular logic devices. In this study, we present a photocleavable DNA nanotube-based dual-amplified resonance Rayleigh scattering (RRS) system for detecting microRNA-126 (miR-126). The cascading dual-amplification biosensing system provides a multilayer-encrypted prototype with the functionality of a molecular computing cascade keypad lock. RRS signals were greatly amplified by using photocleavable DNA nanotubes and enzyme-assisted strand displacement amplification (SDA). In the presence of miR-126, enzyme-assisted SDA produced numerous identical nucleotide fragments as the target, which were then specifically attached to magnetic beads through the DNA nanotube by using a Y-shaped DNA scaffold. Upon ultraviolet irradiation, the DNA nanotube was released into the solution, resulting in an increase in the intensity of the RRS signal. This strategy demonstrated a low limit of detection (0.16 fM) and a wide dynamic range (1 fM to 1 nM) for miR-126. Impressively, the enzyme-assisted SDA offers a molecular computing model for generating the target pool, which serves as the input element for unlocking the system. By cascading the molecular computing process, we successfully constructed a molecular keypad lock with a multilevel authentication technique. The proposed system holds great potential for applications in molecular diagnosis and information security, indicating significant value in integrating molecular circuits for intelligent sensing.

Dual Fluorimetric Sensor for Tandem Detection of Cadmium and Cysteine: An Approach for Designing a Molecular Keypad Lock System.

A fluorimetric sensor for dual and sensitive detection of Cd2+ ion and Cysteine (based on 2-picolylamine platform) was developed.The sensor was designed and synthesized by simple condensation method and characterized by using common spectroscopic methods. The observations made from the kinetics of absorption and emission profile shows that probe Pdac behaves as ''ON-OFF'' fluorescent quenching sensor for cadmium ions. The probe exhibit selectivity in fluorescence quenching behaviour over other competitive metal ions, and also the Pdac-Cd2+ ensemble behave as an efficient ''OFF-ON'' type sensor for an essential amino acid Cysteine. Moreover, this dual sensing nature of the sensor makes it successfully applied for the designing of a molecular keypad lock system.

Host-guest interactions of coumarin-based 1,2-pyrazole using analytical and computational methods: Paper strip-based detection, live cell imaging, logic gates and keypad lock applications

A novel Coumarin-based 1,2-pyrazole, HCPyTSC is synthesised and characterized. The chemosensor has been shown to have efficient colourimetric and fluorescence sensing capabilities for the quick and selective detection of fluoride and copper ions. At 376 and 430 nm, the HCPyTSC exhibits selective sensing for Cu2+ and F− ions. By examining the natural bond orbital (NBO) analysis and the potential energy curve (PES) of the ground state for the function of the C–H bond, it has been determined from the theoretical study at hand that the deprotonation was taken from the ‘CH’ proton of the pyrazole ring. For F− and Cu2+, the HCPyTSC detection limits were 4.62 nM and 15.36 nM, respectively. Similarly, the binding constants (Kb) for F− and Cu2+ ions in acetonitrile medium were found to be 2.06 × 105 M−1 and 1.88 × 105 M−1. Chemosensor HCPyTSC with and without F− and Cu2+ ions have an emission and absorption response that can imitate a variety of logic gates, including the AND, XOR, and OR gates. Additionally, a paper-based sensor strip with the HCPyTSC was created for use in practical, flexible F− sensing applications. The paper-based sensor was more effective in detecting F− than other anions. The effectiveness of HCPyTSC for the selective detection of F− in living cells as well as its cell permeability were examined using live-cell imaging in T24 cells.

A Chromo-fluorogenic Probe for Selective Detection of Picric Acid Alongside Its Recovery by Aliphatic Amines and Construction of Molecular Logic Gates.

Nitroaromatic compounds are illicit explosive chemicals. For environmental security and homeland safety, selective and sensitive identification of these secondary-class explosives has been a reason for the exhaustive research arena of chemists for about a decade. We introduced a sensitive optical sensor with desalted neutral red (NR) dye. After ingressing picric acid (PA) in acetonitrile, the probe becomes non-fluorescent, displaying a colorimetric changefrom yellow to pink. The quenched phenomena and the changed color were re-established with aliphatic amine, trimethylamine (TEA). The reversibility is produced cyclically, both in fluorimetrically and spectrophotometrically. The detection limit for PA with our probe comes out as 0.639µM; this value is significantly lower than many chemosensors available in the literature. Also, NR-stained filter paper strips-based test kit analysis has been deployed as a displayable photonic device for in-situ detection of PA. Furthermore, the whole system was conceptualized to produce single input, single output, and double input single output logic gates, which can be applied to digital devices. The chronological input manner as NTP (NR- TEA-PA) pushed us to configure a molecular keypad lock system, the basis of digital locking devices. The repeatable & reversible detection system exhibits "Write read- Erase-read Write-read' type memory devices.

Engineering a Two-in-one Ni(II)-azophenine switch: Intelligent Lab-on a-box device for decentralized recognition event

A new Ni2+ complex of an azophenine-based sensory receptor, CN-1•Ni2+ is judiciously designed for selective aqueous phase fluoride recognition based on specific hydrogen bonding interaction with sharp chromogenic variation from brownish orange to purple. The mechanistic pathway of interaction has been thoroughly investigated via ESI-MS, FT-IR, differential pulse voltammetry (DPV) studies with theoretical DFT support and Loewdin spin population analysis. The detection limit was acquired to be 148 ppb, which is lower than the WHO permissible limit. The real-time sensitivity of the probe has been displayed by TLC strip-based solid-state sensing assay. The probe is also responsive towards recognition of fluoride from various real field water specimens with promising recoveries (95–119%). One step ahead, the chemically obtained outcomes have been extensively synchronized with electronic circuitry to fabricate lab-on a-box based Layman’s prototype for on-spot, decentralized detection of fluoride, which would be beneficial for the end users, particularly in the fluoride endemic areas. Moreover, based on the reversible spectroscopic outcome, herein AND-NOT-OR-NOR gate-based complex logic circuitry and sequence-dependent molecular keypad lock has been fabricated. In addition, silica gel supported composite material, CN-1•Ni2+@SG has been prepared for effectual remediation of aqueous fluoride below safe limit. Thus, the present work relies on recognition as well as proficient remediation of aqueous fluoride based on selective tuning of acidity, validating the ‘Two-in-one’ approach.

An elaborate biomolecular keypad lock based on electrochromism of viologen derivatives and bioelectrocatalytic reduction of CO2 at supramolecular hydrogel film electrodes

Herein, the short peptide N-fluorenemethoxycarbonyl diphenylalanine (Fmoc-FF) was used to immobilize both diallyl viologen (DAV) and the enzyme formate dehydrogenase (FDH) to form Fmoc-FF/DAV/FDH supramolecular hydrogel films on an electrode surface by a simple solvent-controlled self-assembly method. The DAV component in the films exhibited multiple properties, such as electrochromism and electrofluorochromism, and acted as an electrochemical mediator. A high efficiency of bioelectrocatalytic reduction of CO2 to formate (HCOO−) was obtained by the natural FDH enzyme and the artificial coenzyme factor DAV both immobilized in the same films. The supramolecular hydrogel films with CO2, voltage and light as stimulating factors and current, fluorescence and UV–vis extinction as responsive signals, were further applied for the construction of complex biomolecular logic systems and information encryption. A 3-input/7-output biomolecular logic gate and several logic devices, including an encoder/decoder, a parity checker, and a keypad lock, were constructed. Especially, the biomolecular keypad lock with 3 types of signals as outputs significantly enhanced the security level of information encryption. In this work, a supramolecular self-assembly interface was simply fabricated with complex biomolecular computational functions using immobilized molecules as the computational core, greatly broadening the application range of supramolecular hydrogel films and providing an idea for new designs of bioinformation encryption through the use of a simple film system.

Sequential-Stimuli Induced Stepwise-Response of Pyridylpyrenes.

Stimuli-responsive materials, especially multi-stimuli-responsive materials, can sense external stimuli such as light, heat, and force, have shown great potential in drug delivery, data storage, encryption, energy-harvesting, and artificial intelligence. Conventional multi-stimuli-responsive materials are sensitive to each independent stimulus, causing losses in the diversity and accuracy of the identification for practical application. Herein, a unique phenomenon of sequential-stimuli induced stepwise-response generated from elaborately designed single-component organic materials is reported, which shows large bathochromic shifts up to 5800cm-1 under sequential stimuli of force and light. In contrast to multi-stimuli-responsive materials, the response of these materials strictly relies on the sequence of stimuli, allowing logicality, rigidity, and accuracy to be integrated into one single-component material. The molecular keypad lock is built based on these materials, pointing promising to a future for this logical response in significant practical applications. This breakthrough gives a new drive to classical stimuli-responsiveness and provides a fundamental design strategy for new generations of high-performance stimuli-responsive materials.

Smart Door Lock System by using Mobile via SMS

The concept Door locking and unlocking system uses GPRS to open and close the door. In addition to this the security will be provided using GSM in case of any unauthorized access. The main aim of this project is to provide security at homes, offices etc. The system automatically locks the door as soon as it receives predefined message from the user. The user will have to first register. His information will be stored in database. Whenever the message will be received for the registered number, the controller will accordingly give instruction to DC motor. DC motor will then perform action on door either locking or unlocking. In case of unauthorized access, the IR sensor will sense the action and send the alert message to the registered user using GSM.An OTP-based door lock system is a modern security mechanism that utilizes unique One-Time Passwordsfor secure access. It comprises a microcontroller, GSM module, LCD display, keypad, and solenoid lock. The user enters their mobile number, receives an OTP, and upon successful verification, the door is unlocked. The system is cost-effective, easy to use, and can be installed in various applications for high-security levels. Overall, the OTP-based door lock system provides an efficient alternative to traditional lock-and-key mechanisms for securing access to restricted areas

Multiple stimuli-switchable electrocatalysis and logic gates of l-cysteine based on P(DEA–co-VPBA) hydrogel films

In this work, poly(N',N-diethylacrylamide-co-4-vinylphenylboronic acid) (P(DEA-co-VPBA)) hydrogel films were successfully assembled on the pyrolytic graphite (PG) electrode by a simple radical polymerization. Reversible thermal, glucose and pH-triggered electrochemical reactions were obtained in the presence of 1,1′-ferrocene dicarboxylic acid (FDA) with electro-redox properties. The thermal response performances of the thin-film electrode were attributed to the PDEA component, the sensitive behaviors of glucose were ascribed to the VPBA component, and the sensitive behaviors of pH were affected by PDEA and VPBA. The electrocatalytic oxidation of l-cysteine by FDA on the hydrogel film electrodes significantly enhanced the difference between the on and off states of the multi-response cyclic voltammetry (CV) signals. This smart polymer hydrogel film electrode with amplified signals could be further used to realize a 4-input/9-output binary logic circuit, which was constructed with temperature, glucose, pH, and cysteine as inputs and different levels of Ipa and Ipc responses as outputs. Furthermore, a 2-to-4 decoder, a 4-to-2 encoder, and a 4-input keypad lock were built on the same platform. This polymer electrocatalysis system provides a novel idea for constructing complex biological computing systems.

Intramolecular dual hydrogen bonded fluorescent “turn-on” probe for Al3+ and HSO4- ions: Applications in real water samples and molecular keypad lock

Dual hydrogen bonded Schiff base containing unsymmetrical double proton transfer sites, one with imine bond (CN) and hydroxyl group (OH), and the other with benzimidazole and hydroxyl groups has been successfully synthesized. Probe 1 displayed intramolecular charge transfer and acts as a potential sensor for Al3+ and HSO4- ions. Probe 1 displayed two absorption peaks at 325 nm and 340 nm and an emission band at 435 nm upon excitation at 340 nm. Probe 1 behaves as a fluorescence “turn-on” chemosensor for both Al3+ and HSO4- ions in H2O-CH3OH solvent system. The proposed method allows the determination of Al3+ and HSO4- ions up to 39 nM and 23 nM at emission wavelength 385 nm and 390 nm, respectively. The binding behavior of probe 1 towards these ions is determined by the Job’s plot method and 1H NMR titrations. Probe 1 is used to construct a molecular keypad lock where the absorbance channel can be opened only in the presence of the correct sequence. Further, it is used for the quantitative determination of HSO4- ion in different real-field water samples.

Sequential-Dependent Synthesis of Bimetallic Silver-Chromium Nanoparticles for Multichannel Sensing, Logic Computing, and 3 in 1 Information Protection.

Bimetallic nanomaterials (BNMs) have been used in sensing, biomedicine, and environmental remediation, but their multipurpose and comprehensive applications in molecular logic computing and information security protection have received little attention. Herein, This synthesis method is achieved by sequentially adding reactants under ice bath conditions. Interestingly, Ag-Cr NPs can dynamically selectively sense anions and reductants in multiple channels. Especially, ClO- can be quantitatively detected by oxidizing Ag-Cr NPs with detection limits of 98.37nM (at 270nm) and 31.83nM (at 394nm). Based on sequential-dependent synthesis process of Ag-Cr NPs, Boolean logic gates and customizable molecular keypad locks are constructed by setting the reactants as the inputs, the states of the resulting solutions as the outputs. Furthermore, dynamically selective response patterns of the Ag-Cr NPs can be converted into binary strings to exploit molecular crypto-steganography to encode, store, and hide information. By integrating the three dimensions of authorization, encryption, and steganography, 3 in 1 advanced information protection based on Ag-Cr nanosensing system can be achieved, which can enhance the anti-cracking ability of information. This research will promote the development and application of nanocomposites in the field of information security and deepen the connection between molecular sensing and the information world.

Pilot Study on the Visualization of Latent Fingerprints and Naked Eye Detection of Hg2+ and Zn2+ Ions in Aqueous Media Using Ninhydrin-Based Thiosemicarbazone.

Here, we described a cheap and effective chemosensor (NHPyTSC) that can distinguish Hg2+ and Zn2+ ions from other metal ions and evaluated this phenomenon using several spectroscopy techniques. With the addition of mercury and zinc ions, the proposed chemosensor in particular showed noticeable changes in color and absorption spectra. Additionally, by including EDTA in the NHPyTSC-Hg2+ and NHPyTSC-Zn2+ solutions, colorimetry readings can be reversed. We developed a molecular-scale sequential information processing circuit and presented the "writing-reading-erasing-reading" and "multiwrite" behaviors in the form of binary logic based on the great reversibility of this process. Moreover, by sequentially adding Hg2+, Zn2+, and EDTA, NHPyTSC imitates a molecular keypad lock and molecular logic gates. Density functional theory (DFT) investigations provided more evidence of the Hg2+ and Zn2+ ions' ability to attach to NHPyTSC. The most interesting part of this work is that a study on the latent fingerprint detection of the powder compound revealed that NHPyTSC exhibits good adherence and finger ridge features without background stains. When compared to black and white fingerprint powders, it is discovered that the NHPyTSC powder produces results that are remarkably clear on the majority of surfaces. This demonstrated their potential for real-world use, particularly in the area of criminal investigations.

A simple fluorescent sensor for the meticulous recognition of Cu2+ ion and its functioning in logic gate and keypad lock

A highly selective and perceptive “off–on” mode fluorescent receptor (E)-1-(5-methylfuran-2-yl)-N-(2-(phenylthio)phenyl)methanimine (R) has been constructed for the expeditious recognition of Cu2+ ions in the semi-aqueous medium. The strong fluorescence was observed at 468 nm for Cu2+ ions over other tested metal ions by R, which could be attributed to the constraint of the CHN isomerization mechanism and provoked chelation enhanced fluorescence effect (CHEF) upon interaction with copper ions. According to Job’s plot, the binding proportion between R and copper ion is 2:1 and further validated by mass analysis and quantum chemical studies. Based on the emission titration, the limits of detection (LOD) were determined to be 0.194 μM. The obtained results designate that the receptor R serves as a significant nominee for an expeditious recognition of Cu2+ ions. Further, R was fruitfully useful in molecular keypad locks, and molecular logic gate circuits and it could be applied to find out the trace quantity of Cu2+ ions in water samples.

Facile Label-Free Three-Input Molecular Keypad Lock

Featured with molecule-level data encryption, molecular keypad locks show attractive merits in information security. Most of the previous multiple-input locks use fluorescence as output but are impeded by inefficient/labile prequenching or highly synthetic complexity/difficulty of the fluorophore-containing processor molecules. We herein propose a facile three-input molecular keypad lock, which is simple in synthesis and label free but capable of in situ generation of a fluorescent moiety (dityrosine) for background-free fluorescence readout. A nonfluorescent ("Locked") tyrosine derivate zYpc was easily synthesized as the processor. The correct "password" (i.e., UV → ALP → TYR, ABC) stepwise converted zYpc to a dityrosine-containing product, exhibiting a bright blue fluorescence output ("Open"). In contrast, wrongly permutated inputs failed to open this lock. This device shows potential to be extended as a more advanced keypad lock with better security.