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Molecularly imprinted polymers (MIPs) are pivotal in medicine, mimicking biological receptors with enhanced specificity and affinity. Comprising templates, functional monomers, and cross-linkers, MIPs form stable three-dimensional polymer networks. Synthetic templates like glycan and aptamers improve efficiency, guiding the molecular imprinting process. Cross-linking determines MIPs' morphology and mechanical stability, with printable hydrogels offering biocompatibility and customizable properties, mimicking native extracellular matrix (ECM) microenvironments. Their versatility finds applications in tissue engineering, soft robotics, regenerative medicine, and wastewater treatment. In cancer research, MIPs excel in both detection and therapy. MIP-based detection systems exhibit superior sensitivity and selectivity for cancer biomarkers. They target nucleic acids, proteins, and exosomes, providing stability, sensitivity, and adaptability. In therapy, MIPs offer solutions to challenges like multidrug resistance, excelling in drug delivery, photodynamic therapy, photothermal therapy, and biological activity regulation. In microbiology, MIPs serve as adsorbents in solid-phase extraction (SPE), efficiently separating and enriching antibiotics during sample preparation. They contribute to bacterial identification, selectively capturing specific strains or species. MIPs aid in detecting antibiotic residues using fluorescent nanostructures and developing sensors for sulfadiazine detection in food samples. In summary, MIPs play a pivotal role in advancing medical technologies with enhanced sensitivity, selectivity, and versatility. Applications range from biomarker detection to innovative cancer therapies, making MIPs indispensable for the accurate determination and monitoring of diverse biological and environmental samples.
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Antibacterianos , Polímeros Molecularmente Impressos , Neoplasias , Humanos , Polímeros Molecularmente Impressos/química , Neoplasias/diagnóstico , Antibacterianos/análise , Medicina de Precisão/métodos , Impressão Molecular/métodos , Biomarcadores TumoraisRESUMO
Phyto-derived silver nanoparticles (AgNPs) were modified by three antibiotics including penicillin, amoxicillin, and tetracycline to measure antibacterial activity against Gram-positive and Gram-negative bacteria. According to disc diffusion assay, Staphylococcus aureus exhibited a higher sensitivity compared to Escherichia coli and Pseudomonas aeruginosa under AgNPs/tetracycline stress. Damage of the cell envelops of S. aureus and E. coli as sensitive bacteria under MIC concentrations of Ag NPs/tetracycline was observed by SEM images. AFM technique showed a smaller size of albumin protein (8-13 nm) with a higher level of roughness equals to 74.87 nm relative to hemoglubin (5-6.9 nm) by roughness value of 47.04 nm. Interaction of main secondary metabolites includes nootkatone, nootkatin, daphnauranol C, α-Cyperone, (E)-Nerolidol, and (Z)-α-Bisabolene epoxide surrounding phyto-derived AgNPs with the binding cavities of exfoliative toxin A and exfoliative toxin B as virulence factors of S. aureus was evaluated by molecular docking study. Among these natural compounds, daphnauranol C had the suitable binding affinity as value of - 6.4 kcal/mol compared with other metabolites. Based on the results of this study, tetracycline and daphanuranol C can be considered to further evaluations to obtain novel formulation of AgNPs as an efficient weapon against bacterial infections.
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Antibacterianos , Nanopartículas Metálicas , Albuminas , Amoxicilina , Antibacterianos/química , Escherichia coli/metabolismo , Bactérias Gram-Negativas/metabolismo , Bactérias Gram-Positivas/metabolismo , Hemoglobinas , Nanopartículas Metálicas/química , Testes de Sensibilidade Microbiana , Simulação de Acoplamento Molecular , Penicilinas , Prata/química , Staphylococcus aureus/metabolismo , Tetraciclina/farmacologiaRESUMO
About 80% higher risk of amputation resulted from microbial infection was indicated for patients with diabetic foot ulcers (DFUs). Micro and nano-scaffolds made of natural polymers specifically cellulose, chitosan, and collagen can donate the biocompatibility, biodegradability, and bioavailability properties appropriate to accelerate wound closure before microbial biofilm formation. Antimicrobial activity of these wound dressings can be improved by incorporation of bioactive compounds extracted from medicinal plant species such as curcumin. Low water solubility and poor bioavailability are recognized as two main disadvantages of curcumin, lipophilic phytopolyphenol, which could be controlled by targeted polymeric micro and nano-scaffolds. Consequently, this review has discussed the capacity and challenges of these types of formulations according to recent investigations.
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Curcumina , Nanoestruturas , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Celulose , Quitosana/farmacologia , Colágeno/metabolismo , Curcumina/farmacologia , Curcumina/uso terapêutico , Humanos , Nanoestruturas/uso terapêutico , CicatrizaçãoRESUMO
Antibiotic resistance in pathogenic bacteria to various types of antibiotics has resulted in the necessity of new effective strategies to get around this problem. In recent investigations, metal or metal oxide nanoparticles specifically silver nanoparticles (AgNPs) have been employed successfully to hinder antibiotic-resistant Gram-negative and Gram-positive bacteria. However, AgNPs at high concentrations have cytotoxicity for eukaryotic cells which, application of other biocompatible materials particularly plant secondary metabolites of curcumin and quercetin to reduce cytotoxicity is a critical affair. These compounds may be used directly or indirectly to produce AgNPs. In this regard, modified NPs by curcumin and quercetin have shown an increased therapeutic effect and biocompatibility and biodegredibility properties. Therefore, here, recent advances and challenges about antibacterial and biocompatibility properties of nanoformulation of AgNPs with curcumin and quercetin are presented.
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Curcumina , Nanopartículas Metálicas , Antibacterianos/farmacologia , Bactérias , Curcumina/farmacologia , Testes de Sensibilidade Microbiana , Quercetina/farmacologia , Prata/farmacologiaRESUMO
Polymeric microspheres (MSs) and nanospheres (NSs) composed of synthetic and natural polymers can encapsulate anticancer drugs, among other therapeutics, acting as drug carriers to release them at controlled rates over long periods of time. These carriers present several potential advantages including simple preparation methods, suitable control over the sustained release of medications or stem cells, triggered release resulting from stimulus-responsive delivery, improved physical properties such as porosity and stable scaffolds for tissue engineering, and possible applications as microreactors and nanoreactors compared to conventional drug delivery systems. Moreover, many of these factors can impact drug release rates by polymeric MSs and NSs. Herein, drug delivery systems based on polymeric MSs and NSs are described and compared according to recent advances and challenges, and poignant thoughts on what the field needs to progress are presented.
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Antineoplásicos/química , Microesferas , Nanosferas , Polímeros/química , Portadores de Fármacos/química , Sistemas de Liberação de Medicamentos , Liberação Controlada de Fármacos , Humanos , Tamanho da PartículaRESUMO
Nanotechnology presents the new aspect of material as nanomaterials (NMs) with unique properties such as the large surface area to the volume ratio compared to bulk types. Metal and polymer nanoparticles (NPs) are two major groups of NMs with various medicinal and non-medicinal applications. The rise of antibiotic resistance in microorganisms in general, and bacteria in particular, has necessitated the use of these NMs as novel antibacterial agents. In this regard, medicinal usage of natural polymers particularly cellulose, chitosan, and alginic acid are increasing due to their higher biocompatibility, biodegradability, and accessibility than to other biopolymers or synthetic polymers. Antibacterial activities of these polysaccharides can be improved by incorporation of silver NPs as nanocomposite (NC) forms. Therefore, in this review, recent advances related to nanoformulations of silver NPs with three biopolymers having antibacterial and biocompatibility properties have been discussed.
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Antibacterianos/química , Composição de Medicamentos/tendências , Prata/química , Ácido Algínico/química , Animais , Antibacterianos/farmacologia , Bactérias/efeitos dos fármacos , Bactérias/crescimento & desenvolvimento , Biopolímeros/química , Celulose/química , Quitosana/química , Composição de Medicamentos/métodos , Humanos , Nanopartículas Metálicas/química , Prata/farmacologiaRESUMO
BACKGROUND: Based on gas chromatography - mass spectrometry (GC-MS) results of a previous study, six metabolites including alpha-terpineol, geranyl acetate, linalool, myrcenol, terpinolene, and thymol showed significantly higher amounts relative to other metabolites. METHODS: A continuation of the previous study, the interaction of these metabolites with the main virulence factors of P. aeruginosa (pseudomonas elastase and exotoxin A), Staphylococcus aureus (alpha-hemolysin and protein 2a), Mycobacterium tuberculosis (ESX-secreted protein B and the serine/threonine protein kinase), and Escherichia coli (heat-labile enterotoxin and Shiga toxin) were evaluated by molecular docking study and molecular simulation. RESULTS: In the case of Shiga toxin, higher and lower binding affinities were related to alpha-terpinolene and zincite with values of -5.8 and -2.6 kcal/mol, respectively. For alpha-hemolysin, terpinolene and alpha-terpinolene demonstrated higher binding affinities with similar energies of -5.9 kcal/mol. Thymol and geranyl acetate showed lower binding energy of -5.7 kcal/mol toward protein 2a. Furthermore, thymol had a higher binding affinity toward heat-labile enterotoxin and ESX-secreted protein B with values of -5.9 and -6.1 kcal/mol, respectively. CONCLUSIONS: It is concluded that the availability of secondary metabolites of A. haussknechtii surrounding zinc oxide (ZnO) NPs can hinder P. aeruginosa by inactivating Pseudomonas elastase and exotoxin.
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Acetatos , Monoterpenos Acíclicos , Monoterpenos Cicloexânicos , Monoterpenos , Mycobacterium tuberculosis , Octanóis , Infecções Estafilocócicas , Humanos , Timol/química , Staphylococcus aureus , Pseudomonas aeruginosa , Simulação de Acoplamento Molecular , Fatores de Virulência , Escherichia coli , Proteínas Hemolisinas , Enterotoxinas , Exotoxinas , Toxinas Shiga , Elastase PancreáticaRESUMO
INTRODUCTION: Nanocomposites based on copper, iron, and carbon materials are novel nanomaterials with both antibacterial and biocompatibility properties considerable to fight against multidrug-resistant bacteria. METHODS: In this study, phytogenic carbon/FeSO4/Cu/CuO nanocomposites modified by three antibiotics including tetracycline, amoxicillin, and penicillin were employed to hinder antibiotic resistant bacteria of Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. Interaction of albumin and hemoglobin as major blood proteins with these nanocomposites were evaluated by SEM, FTIR, and AFM techniques. As in silico study, molecular docking properties of staphylococcal enterotoxin toxin A and B with (Z)-α-Bisabolene epoxide, (E)-Nerolidol, α-Cyperone, daphnauranol C, nootkatin, and nootkatone as major secondary metabolites of Daphne mucronata were obtained by AutoDock Vina program. RESULTS: Physicochemical characterization of nanocomposites showed (Zeta potential (- 5.09 mV), Z-average (460.2 d.nm), polydispersity index (0.293), and size range of 44.58 ± 6.78 nm). Results of both in vitro and in silico surveys disclosed significant antibacterial activity of antibiotic functionalized carbon/FeSO4/Cu/CuO nanocomposites compared to antibiotics alone towards Gram-negative and Gram-positive bacteria. CONCLUSION: Synergistic activity of bio-fabricated carbon/FeSO4/Cu/CuO nanocomposites with antibiotics may be affected by main parameters of concentration and ratio of antibacterial agents, physicochemical properties of nanocomposites, bacterial type (Gram-negative or Gram-positive), antibacterial mechanisms, and chemical structure of antibiotics.
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Introduction: Nanoparticles (NPs) are of great interest in the design of various drugs due to their high surface-to-volume ratio, which result from their unique physicochemical properties. Because of the importance of examining the interactions between newly designed particles with different targets in the case of various diseases, techniques for examining the interactions between these particles with different targets, many of which are proteins, are now very common. Methods: In this study, the interactions between metal oxide nanoparticles (MONPs) covered with a carbon layer (Ag2O3, CdO, CuO, Fe2O3, FeO, MgO, MnO, and ZnO NPs) and standard drugs related to the targets of Cancer and bacterial infections were investigated using the molecular docking technique with AutoDock 4.2.6 software tool. Finally, the PRO TOX-II online tool was used to compare the toxicity (LD50) and molecular weight of these MONPs to standard drugs. Results: According to the data obtained from the semi flexible molecular docking process, MgO and Fe2O3 NPs performed better than standard drugs in several cases. MONPs typically have a lower 50% lethal dose (LD50) and a higher molecular weight than standard drugs. MONPs have shown a minor difference in binding energy for different targets in three diseases, which probably can be attributed to the specific physicochemical and pharmacophoric properties of MONPs. Conclusion: The toxicity of MONPs is one of the major challenges in the development of drugs based on them. According to the results of these molecular docking studies, MgO and Fe2O3 NPs had the highest efficiency among the investigated MONPs.
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INTRODUCTION: The inactivation and eradication of multidrug-resistant bacteria, fungi, and viruses by conventional antibiotics and drugs have not been effective. The hindering of these pathogens in hospital-acquired infections caused by Gram-positive bacteria, particularly strains of S. aureus including community-acquired methicillin-resistant (CA-MRSA) and hospital-acquired MRSA (HA-MRSA), is more complicated, specifically in patients having immunodeficiency syndrome. RESEARCH AREA: Bare and functionalized metal and metal oxide nanoparticles (NPs) specifically silver (Ag) NPs have shown significant antibacterial, antifungal, and antiviral activities. Biosynthesis of AgNPs by fungal species in media of cell-free filtrate and culture supernatant can provide new therapeutic properties compared to physical and chemical methods. EXPERT OPINION: Various primary and secondary metabolites of fungi such as phytochelatin, trichodin, primin, altersolanol A, periconicin A, brefeldin A, graphislactone A, phomol, polysaccharides (chitin, glucans, and galactomannans), and enzymes can contribute to reducing Ag+ ions and stabilizing NPs in one-pot method. These natural compounds can augment antimicrobial activity by bypassing multidrug-resistance barriers in viruses, bacteria, and fungi. Controlling physicochemical properties and effective therapeutic concentration of fungal AgNPs can be the determinative parameters for the antimicrobial strength of AgNPs. Therefore, in this review, we have tried to address the antimicrobial mechanisms and physicochemical properties of fungal synthesized AgNPs.
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Anti-Infecciosos , Nanopartículas Metálicas , Humanos , Staphylococcus aureus , Antibacterianos/farmacologia , Anti-Infecciosos/farmacologia , Bactérias , Nanopartículas Metálicas/química , Testes de Sensibilidade MicrobianaRESUMO
Brucellosis, a zoonotic intracellular bacterial infection primarily transmitted through the consumption of unpasteurized milk from infected animals, remains a challenging condition to clinically control. This is mainly because of the limited effectiveness of conventional antibiotics in targeting intracellular Brucella. Micro- and nanoformulations of antibiotics, whether used as a mono- or combination therapy, have the potential to reduce the antibiotic doses required and treatment duration. Extensive research has been conducted on various organic, semiorganic, and inorganic nanomaterials with different morphologies, such as nanoparticles (NPs), nanotubes, nanowires, and nanobelts. Metal/metal oxide, lipidic, polymeric, and carbonic NPs have been widely explored to overcome the limitations of traditional formulations. In this review, we discuss the advances and challenges of these novel formulations based on recent investigations.
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Brucella , Brucelose , Animais , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Brucelose/tratamento farmacológico , Brucelose/microbiologiaRESUMO
Antibiotic resistance of bacteria has caused a significant public health challenge and economic problem, resulting in a necessity to find efficient antibacterial agents. Conventional bactericidal agents hinder the growth of bacteria by slowing down the cell wall synthesis or disturbing bacterial DNA replication, protein production or other bacterial cellular metabolism that can augment natural selection pressure for turning up new antibiotic-resistant strains. Virulence properties and biofilm formation of bacteria are orchestrated by quorum-sensing systems. These quorum-sensing systems normally control antimicrobial production; and targeting these systems using metal-based nanoparticles or polymeric nanoparticles can be considered as powerful antibacterial treatments owing to their specific physicochemical and therapeutic properties. In this review, recent advances and challenges related to the inactivation of quorum-sensing systems by these nanoparticles are presented to obtain comprehensive viewpoints for future studies.
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Nanopartículas Metálicas , Percepção de Quorum , Percepção de Quorum/fisiologia , Biofilmes , Bactérias , Antibacterianos/uso terapêutico , Metais , ÓxidosRESUMO
Quantum dots (QDs) are semiconductor materials that range from 2 nm to 10 nm. These nanomaterials (NMs) are smaller and have more unique properties compared to conventional nanoparticles (NPs). One of the unique properties of QDs is their special optoelectronic properties, making it possible to apply these NMs in bioimaging. Different size and shape QDs, which are used in various fields such as bioimaging, biosensing, cancer therapy, and drug delivery, have so far been produced by chemical methods. However, chemical synthesis provides expensive routes and causes serious environmental and health issues. Therefore, various biological systems such as bacteria, fungi, yeasts, algae, and plants are considered as potent eco-friendly green nanofactories for the biosynthesis of QDs, which are both economic and environmentally safe. The review aims to provide a descriptive overview of the various microbial agents for the synthesis of QDs and their biomedical applications for the diagnosis and treatment of cancer and SARS-CoV-2.
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The future of molecular-level therapy, efficient medical diagnosis, and drug delivery relies on the effective theragnostic function which can be achieved by the synergistic effect of fluorescent carbon dots (FCDs) liposomes (L) and nanoliposomes. FCDs act as the excipient navigation agent while liposomes play the role of the problem-solving agent, thus the term "theragnostic" would describe the effect of LFCDs properly. Liposomes and FCDs share some excellent at-tributes such as being nontoxic and biodegradable and they can represent a potent delivery system for pharmaceutical compounds. They enhance the therapeutic efficacy of drugs via stabilizing the encapsulated material by circumventing barriers to cellular and tissue uptake. These agents facilitate long-term drug biodistribution to the intended locations of action while eliminating systemic side effects. This manuscript reviews recent progress with liposomes, nanoliposomes (collectively known as lipid vesicles) and fluorescent carbon dots, by exploring their key characteristics, applications, characterization, performance, and challenges. An extensive and intensive understanding of the synergistic interaction between liposomes and FCDs sets out a new research pathway to an efficient and theragnostic / theranostic drug delivery and targeting diseases such as cancer.
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Lipossomos , Fotoquimioterapia , Carbono , Distribuição Tecidual , Fotoquimioterapia/métodos , Fármacos Fotossensibilizantes , CorantesRESUMO
INTRODUCTION: Mitigation of infectious diseases resulted from antibiotic-resistant bacteria is difficult by current antibiotics. Metal and metal oxide nanoparticles specifically Ag nanoparticles can be efficient antibacterial agents considering their biocompatibility. In this way, biosynthesis of Ag nanoparticles by living organisms or their metabolites has obtained more attention compared to chemical or physical methods. AREAS COVERED: Bacteria and fungi in extracellular and intracellular pathways and related primary and secondary metabolites can synthesize Ag nanoparticles with synergistic antibacterial activity against bacterial pathogens. EXPERT OPINION: Bacteriostatic and bactericidal effects of these nanoparticles can lead by production of reactive oxygen species and inactivation of biological macromolecules such as proteins and nucleic acids. The present review has tried to discuss recent progress and challenges about biosynthesis mechanisms and antibacterial activity of Ag nanoparticles bio-inspired by archaebacteria, actinomycetes, cyanobacteria, and fungi.
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Nanopartículas Metálicas , Prata , Antibacterianos/química , Antibacterianos/farmacologia , Bactérias , Fungos , Humanos , Nanopartículas Metálicas/química , Testes de Sensibilidade Microbiana , Óxidos , Prata/farmacologiaRESUMO
The diterpenoid molecule paclitaxel (PTX), extracted from the Western yew tree, Taxus brevifolia, is a promising anticancer drug specifically in clinical use for ovarian and breast cancers. However, its wider use is hampered by adverse effects and emerging resistance in cancer cells. Micelles, liposomes, cubosomes, and lipid nanoparticles (LNPs) have the potential to reduce or even remove complications associated with the use of PTX. Herein, we provide an overview of micro- and nanoformulations of PTX based on micelles, liposomes, cubosomes and LNPs to improve the therapeutic effects of this drug both in vitro and in vivo.
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Nanopartículas , Paclitaxel , Linhagem Celular Tumoral , Portadores de Fármacos , Humanos , Lipossomos , Micelas , Paclitaxel/uso terapêutico , PolietilenoglicóisRESUMO
Certain types of metal-based nanoparticles are effective antiviral agents when used in their original form ("bare") or after their surfaces have been functionalized ("modified"), including those comprised of metals (e.g., silver) and metal oxides (e.g., zinc oxide, titanium dioxide, or iron dioxide). These nanoparticles can be prepared with different sizes, morphologies, surface chemistries, and charges, which leads to different antiviral activities. They can be used as aqueous dispersions or incorporated into composite materials, such as coatings or packaging materials. In this review, we provide an overview of the design, preparation, and characterization of metal-based nanoparticles. We then discuss their potential mechanisms of action against various kinds of viruses. Finally, the applications of some of the most common metal and metal oxide nanoparticles are discussed, including those fabricated from silver, zinc oxide, iron oxide, and titanium dioxide. In general, the major antiviral mechanisms of metal and metal oxide nanoparticles have been observed to be 1) attachment of nanoparticles to surface moieties of viral particles like spike glycoproteins, that disrupt viral attachment and uncoating in host cells; 2) generation of reactive oxygen species (ROS) that denature viral macromolecules such as nucleic acids, capsid proteins, and/or lipid envelopes; and 3) inactivation of viral glycoproteins by the disruption of the disulfide bonds of viral proteins. Several physicochemical properties of metal and metal oxide nanoparticles including size, shape, zeta potential, stability in physiological conditions, surface modification, and porosity can all impact the antiviral efficacy of the nanoparticles.
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Nanopartículas Metálicas , Óxido de Zinco , Antivirais/farmacologia , Nanopartículas Metálicas/química , Óxidos/química , Óxidos/farmacologia , Prata , Óxido de Zinco/químicaRESUMO
Severe acute respiratory syndrome (SARS)-CoV-2 from the family Coronaviridae is the cause of the outbreak of severe pneumonia, known as coronavirus disease 2019 (COVID-19), which was first recognized in 2019. Various potential antiviral drugs have been presented to hinder SARS-CoV-2 or treat COVID-19 disease. Side effects of these drugs are among the main complicated issues for patients. Natural compounds, specifically primary and secondary herbal metabolites, may be considered as alternative options to provide therapeutic activity and reduce cytotoxicity. Phenolic materials such as epigallocatechin gallate (EGCG, polyphenol) and quercetin have shown antibacterial, antifungal, antiviral, anticancer, and anti-inflammatory effects in vitro and in vivo. Therefore, in this study, molecular docking was applied to measure the docking property of epigallocatechin gallate and quercetin towards the transmembrane spike (S) glycoprotein of SARS-CoV-2. Results of the present study showed Vina scores of -9.9 and -8.3 obtained for EGCG and quercetin by CB-Dock. In the case of EGCG, four hydrogen bonds of OG1, OD2, O3, and O13 atoms interacted with the Threonine (THR778) and Aspartic acid (ASP867) amino acids of the spike glycoprotein (6VSB). According to these results, epigallocatechin gallate and quercetin can be considered potent therapeutic compounds for addressing viral diseases.
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Ag and ZnO nanoparticles (NP) can be prepared by physical, chemical, or eco-friendly methods. The biosynthesis of metal and metal oxide NPs by plants, fungi, and bacteria could be a promising way to obtain biocompatible NPs that have desirable antibacterial activities. However, the uniformity of shape, size, and size distribution of NPs are crucial to producing significant antibacterial results, particularly in physiological conditions such as infected wounds or septicemia. In this review, we discuss recent progress and challenges in the use of novel approaches for the biosynthesis of Ag and ZnO nanoparticles that have antibacterial activities.
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Antibacterianos/isolamento & purificação , Nanopartículas Metálicas/química , Antibacterianos/química , Antibacterianos/farmacologia , Bactérias/metabolismo , Fungos/metabolismo , Humanos , Plantas Medicinais/metabolismo , Prata/química , Prata/isolamento & purificação , Óxido de Zinco/química , Óxido de Zinco/isolamento & purificaçãoRESUMO
INTRODUCTION: Emergence of antibiotic resistance in bacteria is a complicated issue, especially when treating infectious immunodeficiency related diseases. In recent years, when compared to bulk materials, nanomaterials (NMs) with specific antibacterial activities have played a novel role in treating bacterial infections. Among NMs, quantum dots (QDs), specifically carbon containing QDs including graphene oxide QD (GOQD), graphene QD (GQD), and carbon QD (CQD), have demonstrated bacteriostatic and bactericidal activities via photodynamic (PD) effects against antibiotic resistant bacteria under a certain wavelength of light. AREA COVERED: In this mini-review, recent advances and challenges related to antibacterial and biocompatibility activities of modified GQD, GOQD, CQD, and carbon nanotubes (CNTs) are discussed. EXPERT OPINION: Lower stability and biocompatibility of QDs at higher doses in physiological conditions are major disadvantages. In this regard, functionalization of these QDs can result in appropriate bactericidal, biocompatibility, and biodegradability properties. In the case of CNTs including single-wall carbon nanotube (SWCNTs) and multiwall carbon nanotube (MWCNTs), aspect ratio (AR) is a determinant factor for the antibacterial value. Moreover, MWCNTs show a lower antibacterial ability compared to SWCNTs, which can be improved by modifying their surface.