Rapid synthesis of highly monodisperse AgSbS₂ nanocrystals: unveiling multifaceted activities in cancer therapy, antibacterial strategies, and antioxidant defense

• Funda Ulusu,
• Adem Sarilmaz,
• Yakup Ulusu,
• Faruk Ozel and
• Mahmut Kus

Beilstein J. Nanotechnol. 2025, 16, 2105–2115, doi:10.3762/bjnano.16.145

• effects by efficiently eliminating DPPH activity. This research highlights the potential of AgSbS2 NCs as versatile agents with applications in biomedical and environmental domains, including cancer therapy, antimicrobial strategies, and free radical neutralization. Keywords: AgSbS2 nanocrystals

Toward clinical translation of carbon nanomaterials in anticancer drug delivery: the need for standardisation

• Michał Bartkowski,
• Francesco Calzaferri and
• Silvia Giordani

Beilstein J. Nanotechnol. 2025, 16, 2092–2104, doi:10.3762/bjnano.16.144

• updated every decade [23][24]. The hallmarks framework has enabled researchers to develop more nuanced, spatially informed approaches to cancer therapy, reinforcing its role in driving multidisciplinary strategies for predicting treatment response [25]. Targeted drug delivery is an emerging

• nanoscale materials, highlighting key agencies, legislative instruments, and guidance initiatives. Supporting Information Supporting Information File 18: Overview of conventional drug delivery methods in cancer therapy, including administration routes, key characteristics, and example drugs. Funding The

Exploring the potential of polymers: advancements in oral nanocarrier technology

• Rousilândia de Araujo Silva,
• Igor Eduardo Silva Arruda,
• Luise Lopes Chaves,
• Mônica Felts de La Roca Soares and
• Jose Lamartine Soares Sobrinho

Beilstein J. Nanotechnol. 2025, 16, 1751–1793, doi:10.3762/bjnano.16.122

• widely utilized in cancer therapy due to their specific ability to regulate the expression of any associated gene [141] the findings of Han et al. [117] represent an effective approach for synergistic therapy via oral RNA delivery. Moreover, these findings open new possibilities for the application of

Advances of aptamers in esophageal cancer diagnosis, treatment and drug delivery

• Yang Fei,
• Hui Xu,
• Chunwei Zhang,
• Jingjing Wang and
• Yong Jin

Beilstein J. Nanotechnol. 2025, 16, 1734–1750, doi:10.3762/bjnano.16.121

• . Pegaptanib and Avacincaptad pegol can be administered topically by intravitreal injection, easily achieving ideal bioavailability. However, the clinical utility of aptamer-based therapeutics remains limited. Developing new aptamers for esophageal cancer therapy presents multiple challenges, such as lack of

• first peptide aptamer was proposed in 1996 to recognize and inhibit cyclin dependent kinase 2 (Cdk2) [68]. Later, peptide aptamers were used directly as drugs to regulate proteins and genes [69][70][71], showing potential in the field of targeted cancer therapy. Transcription factor SOX2, as a lineage

Prospects of nanotechnology and natural products for cancer and immunotherapy

• Jan Filipe Andrade Santos,
• Marcela Bernardes Brasileiro,
• Pamela Danielle Cavalcante Barreto,
• Ligiane Aranha Rocha and
• José Adão Carvalho Nascimento Júnior

Beilstein J. Nanotechnol. 2025, 16, 1644–1667, doi:10.3762/bjnano.16.116

• pharmacokinetic properties, increasing bioavailability, protecting them from degradation, and allowing for site-specific delivery [24]. Consequently, this combination addresses both the limitations of natural products and the complex challenges of cancer therapy [25]. Unlike conventional literature reviews, this

• effects, which could contribute to cancer prevention and treatment [135]. In cancer therapy, PCs show potential for inhibiting cancer cell proliferation, inducing apoptosis, modulating oxidative stress, suppressing angiogenesis, and interfering with signaling pathways involved in tumor progression [136

• possesses a combination of properties that include antioxidant and antitumor effect, giving it potential to prevent and/or treat cancer by stimulating apoptosis [144]. Meanwhile, glucan presents potential in cancer therapy due to its immunomodulatory influence, which can increase the recruitment of

Nanomaterials for biomedical applications

• Iqra Zainab,
• Zohra Naseem,
• Syeda Rubab Batool,
• Filippo Pierini,
• Seda Kizilel and
• Muhammad Anwaar Nazeer

Beilstein J. Nanotechnol. 2025, 16, 1499–1503, doi:10.3762/bjnano.16.105

• membranes [8]. They can carry both water-soluble and fat-soluble drugs, shielding them from breaking down and extending their circulation time. Certain liposome-based drugs have already been approved for therapeutic use, especially in cancer therapy, where they may protect nearby healthy cells from toxicity

Ferroptosis induction by engineered liposomes for enhanced tumor therapy

• Alireza Ghasempour,
• Mohammad Amin Tokallou,
• Mohammad Reza Naderi Allaf,
• Mohsen Moradi,
• Hamideh Dehghan,
• Mahsa Sedighi,
• Mohammad-Ali Shahbazi and
• Fahimeh Lavi Arab

Beilstein J. Nanotechnol. 2025, 16, 1325–1349, doi:10.3762/bjnano.16.97

• tumor therapy. It also highlights the fascinating outcome of liposome-mediated ferroptosis in overcoming the obstacles to cancer therapy, along with the limitations and possible future directions. Keywords: cancer; ferroptosis; liposome; nanomedicine; stimuli-responsive; Review 1 Introduction Cancer

• accumulation of lipid ROS. Ferroptosis clearly differs from necrosis, apoptosis, and autophagy in terms of cellular morphology and function [7]. Recently, studies have indicated that ferroptosis can be utilized for cancer therapy since it effectively eliminates cancer cells and reverses drug resistance [8][9

• advantages and impact on cancer therapy and diagnosis [17]. Therapies based on nanotechnology, such as the progressive delivery of nanoscale drugs, can provide precisely targeted treatment of malignant tissue with fewer side effects than traditional approaches [5][18]. Key benefits of nanodrug delivery

Better together: biomimetic nanomedicines for high performance tumor therapy

• Imran Shair Mohammad,
• Gizem Kursunluoglu,
• Anup Kumar Patel,
• Hafiz Muhammad Ishaq,
• Cansu Umran Tunc,
• Dilek Kanarya,
• Mubashar Rehman,
• Omer Aydin and
• Yin Lifang

Beilstein J. Nanotechnol. 2025, 16, 1246–1276, doi:10.3762/bjnano.16.92

Hydrogels and nanogels: effectiveness in dermal applications

• Jéssica da Cruz Ludwig,
• Diana Fortkamp Grigoletto,
• Daniele Fernanda Renzi,
• Wolf-Rainer Abraham,
• Daniel de Paula and
• Najeh Maissar Khalil

Beilstein J. Nanotechnol. 2025, 16, 1216–1233, doi:10.3762/bjnano.16.90

• optimized nanogel-MTX combines the characteristics of biocompatibility, sustained systemic release, safety, and efficacy in the treatment of rheumatoid arthritis in a single system [193]. Nanogels and hydrogels applied to skin cancer therapy Therapy against skin cancer has been a major focus for the

• [220][221]. Ethosomal nanogels containing sulforaphane, a potent natural antioxidant [222], showed a significant anti-cancer effect (p < 0.05) in murine tumor cell type B16-F10, proven to be an attractive strategy for skin cancer therapy [192]. A hydrogel system based on oligopeptides and embedded

• nanocarriers, facilitating industrial manufacturing. Hydrogels, used in dermatological treatment such as wound healing films, advance the commercialization of hydrogel-based medicines. Nanogels, aiding targeted delivery, enhance the efficacy of skin cancer therapy. Their biocompatibility and ability to mimic

Synthesis and magnetic transitions of rare-earth-free Fe–Mn–Ni–Si-based compositionally complex alloys at bulk and nanoscale

• Shabbir Tahir,
• Tatiana Smoliarova,
• Carlos Doñate-Buendía,
• Michael Farle,
• Natalia Shkodich and
• Bilal Gökce

Beilstein J. Nanotechnol. 2025, 16, 823–836, doi:10.3762/bjnano.16.62

• applications such as magnetic hyperthermia, where NPs are used in cancer therapy to induce localized heating when exposed to an alternating magnetic field [34]. However, producing CCAs at the nanoscale presents significant challenges. Traditional wet chemistry approaches often fail because of elemental

Polyurethane/silk fibroin-based electrospun membranes for wound healing and skin substitute applications

• Iqra Zainab,
• Zohra Naseem,
• Syeda Rubab Batool,
• Muhammad Waqas,
• Ahsan Nazir and
• Muhammad Anwaar Nazeer

Beilstein J. Nanotechnol. 2025, 16, 591–612, doi:10.3762/bjnano.16.46

• growth [175]. Zhou et al. focused on the fabrication of a novel composite membrane suitable for photothermal cancer therapy based on black phosphorus (BP) nanosheets because of their high biocompatibility and photothermal efficacy. SF was used as an exfoliating agent in stable liquid exfoliation with

Synthetic-polymer-assisted antisense oligonucleotide delivery: targeted approaches for precision disease treatment

• Ana Cubillo Alvarez,
• Dylan Maguire and
• Ruairí P. Brannigan

Beilstein J. Nanotechnol. 2025, 16, 435–463, doi:10.3762/bjnano.16.34

• systems for cancer therapy, Kim et al. employed PLL in the synthesis of dually stabilised triblock copolymer micelles for the systemic delivery of phosphorothioate ASOs (metastasis associated lung adenocarcinoma transcript 1 lncRNA-targeted ASO (MALAT1-ASO) and GL3 luciferase-targeted ASO (GL3-ASO

Nanocarriers and macrophage interaction: from a potential hurdle to an alternative therapeutic strategy

• Naths Grazia Sukubo,
• Paolo Bigini and
• Annalisa Morelli

Beilstein J. Nanotechnol. 2025, 16, 97–118, doi:10.3762/bjnano.16.10

• the context. In cancer therapy, reprogramming M2 macrophages into M1 enhances antitumor immunity, while in chronic inflammatory diseases, shifting from M1 to M2 facilitates inflammation resolution and tissue repair. This modulation can be achieved using small molecules, cytokines, or nanotechnology to

• target key signaling pathways [62]. M1 polarization in cancer therapy: Inducing or sustaining M1 polarization has proven effective in enhancing antitumor immunity. For example, chimeric antigen receptor macrophages (CAR-Ms), engineered by Klichinsky et al., sustained a robust M1 phenotype for over 40

• polarization by targeting TERF2IP, activating STAT3, and inhibiting NF-κB [70][71]. Innovative delivery systems for miRNAs have further advanced their therapeutic application. Liu et al. developed a hybrid nanovector with dual redox/pH-responsive properties for targeted miRNA delivery in cancer therapy. This

Biomimetic nanocarriers: integrating natural functions for advanced therapeutic applications

• Hugo Felix Perini,
• Beatriz Sodré Matos,
• Carlo José Freire de Oliveira and
• Marcos Vinicius da Silva

Beilstein J. Nanotechnol. 2024, 15, 1619–1626, doi:10.3762/bjnano.15.127

• targeting specificity. Biomimetic nanocarriers demonstrate significant advancements in drug delivery systems against cancer therapy, Alzheimer's disease, autoimmune diseases, and viral infections such as COVID-19. Here, we address the therapeutic applications of biomimetic nanocarriers and their promising

• drug delivery in cancer therapy has been extensively studied in the pursuit of biocompatible components with high specificity. In this context, the integration of synthetic compounds such as nanoparticles with natural components, including membranes from various cell types (e.g., erythrocytes

Polymer lipid hybrid nanoparticles for phytochemical delivery: challenges, progress, and future prospects

• Iqra Rahat,
• Pooja Yadav,
• Aditi Singhal,
• Mohammad Fareed,
• Jaganathan Raja Purushothaman,
• Mohammed Aslam,
• Raju Balaji,
• Sonali Patil-Shinde and
• Md. Rizwanullah

Beilstein J. Nanotechnol. 2024, 15, 1473–1497, doi:10.3762/bjnano.15.118

• therapeutic efficacy [44]. The development of PLHNPs for phytochemical delivery holds significant promise across various biomedical applications. PLHNPs can be utilized in cancer therapy, cardiovascular disease management, neurodegenerative disorder treatment, and other areas of medicine where phytochemicals

• in cancer therapy. This targeted delivery can increase the therapeutic efficacy of drugs while reducing side effects by minimizing off-target effects [61][62]. For instance, Garg et al. fabricated fucose ligand-decorated PLHNPs for the co-delivery of methotrexate and aceclofenac to achieve targeted

• and lipid-based carriers, providing stability, biocompatibility, and efficient drug encapsulation. Applications of stimuli-responsive PLHNPs are vast and impactful. In cancer therapy, they are used to deliver chemotherapeutic agents specifically to tumor sites, where the acidic microenvironment or

Unveiling the potential of alginate-based nanomaterials in sensing technology and smart delivery applications

• Shakhzodjon Uzokboev,
• Khojimukhammad Akhmadbekov,
• Ra’no Nuritdinova,
• Salah M. Tawfik and
• Yong-Ill Lee

Beilstein J. Nanotechnol. 2024, 15, 1077–1104, doi:10.3762/bjnano.15.88

Therapeutic effect of F127-folate@PLGA/CHL/IR780 nanoparticles on folate receptor-expressing cancer cells

• Thi Ngoc Han Pham,
• Phuong-Thao Dang-Luong,
• Hong-Phuc Nguyen,
• Loc Le-Tuan,
• Xuan Thang Cao,
• Thanh-Danh Nguyen,
• Vy Tran Anh and
• Hieu Vu_Quang

Beilstein J. Nanotechnol. 2024, 15, 954–964, doi:10.3762/bjnano.15.78

• ). Additionally, the F127-folate@PLGA/CHL/IR780 nanoparticles exhibited a lower IC50 value against cancer cells than non-targeted F127@PLGA/CHL/IR780 nanoparticles. These findings suggest that the developed F127-folate@PLGA/CHL/IR780 nanoparticles hold promise as a theragnostic system for targeted cancer therapy

• on the half-life of nanoparticles that are currently in circulation. The optimal nanoparticle size for cancer therapy was observed to vary between 50 and 200 nm [39][40]. In our study, the nanoparticles were tailored for in vivo drug administration; thus, our nanoparticle size was suitable for use in

Electrospun polysuccinimide scaffolds containing different salts as potential wound dressing material

• Veronika Pálos,
• Krisztina S. Nagy,
• Rita Pázmány,
• Krisztina Juriga-Tóth,
• Bálint Budavári,
• Judit Domokos,
• Dóra Szabó,
• Ákos Zsembery and
• Angela Jedlovszky-Hajdu

Beilstein J. Nanotechnol. 2024, 15, 781–796, doi:10.3762/bjnano.15.65

• )/hydroxyapatite in orthopedics [1][2]. Biocompatible polymers are widely used in biomedical fields, such as stents, drug delivery systems in cancer therapy, bone repair, dentistry, joint prostheses, and tissue engineering [2][3][4][5][6]. Polymers have several advantageous properties for these applications as

Vinorelbine-loaded multifunctional magnetic nanoparticles as anticancer drug delivery systems: synthesis, characterization, and in vitro release study

• Zeynep Özcan and
• Afife Binnaz Hazar Yoruç

Beilstein J. Nanotechnol. 2024, 15, 256–269, doi:10.3762/bjnano.15.24

• cancer therapy agent, is included in the nanocomposite structure, and in vitro drug release studies under different pH conditions (pH 5.5 and 7.4) and photothermal activity at 808 nm NIR laser irradiation are investigated. The comprehensive integration of precise multifunctional nanoparticles design

• ’ magnetization cycle, as Bloch and Neel theorized [11][13]. Superparamagnetic iron oxide nanoparticles for drug delivery, diagnosis, and cancer therapy have gained wider acceptance in biomedical applications [14]. They have received notable attention in clinical applications such as early disease diagnosis (e.g

• of passive targeting in magnetic fields for photothermal cancer therapy, with PDA holds great promise for future applications. Therefore, surface modification with PDA is recognized as a favorable alternative for enhancing the biocompatibility of non-biodegradable substances. A study focused on

Nanocarrier systems loaded with IR780, iron oxide nanoparticles and chlorambucil for cancer theragnostics

• Phuong-Thao Dang-Luong,
• Hong-Phuc Nguyen,
• Loc Le-Tuan,
• Xuan-Thang Cao,
• Vy Tran-Anh and
• Hieu Vu Quang

Beilstein J. Nanotechnol. 2024, 15, 180–189, doi:10.3762/bjnano.15.17

• shown the potential application not only for cancer therapy but also for diagnosis. First, the NPs are internalized into the cells and gradually degrade in the low pH of the endosomes releasing CHL to interrupt the cell cycle. Second, the NPs carry both imaging agents, IR780 and IO, which are suitable

Curcumin-loaded albumin submicron particles with potential as a cancer therapy: an in vitro study

• Nittiya Suwannasom,
• Netsai Sriaksorn,
• Chutamas Thepmalee,
• Krissana Khoothiam,
• Ausanai Prapan,
• Hans Bäumler and
• Chonthida Thephinlap

Beilstein J. Nanotechnol. 2023, 14, 1127–1140, doi:10.3762/bjnano.14.93

• to confirm the uptake of CUR-HSA-MPs by cancer cells. Our studies revealed that HSA-MPs are potentially promising vehicles for increasing the solubility and bioavailability of CUR. Keywords: albumin submicron particles; cancer therapy; curcumin; drug delivery; Introduction Curcumin (CUR) is a

• into cancer cells, making them a promising option for cancer therapy. In addition, the surface modification of microparticles using substances such as antibodies and polymers suggests the potential for enhanced uptake, as previously demonstrated [55][56]. Nevertheless, further research should explore

Nanoarchitectonics of photothermal materials to enhance the sensitivity of lateral flow assays

• Elangovan Sarathkumar,
• Rajasekharan S. Anjana and
• Ramapurath S. Jayasree

Beilstein J. Nanotechnol. 2023, 14, 988–1003, doi:10.3762/bjnano.14.82

• change [20][21]. Generally, photothermal nanomaterials are being used in cancer therapy, removal of bacterial biofilms, and sensing applications [22][23][24]. Photothermal nanomaterials produce heat in response to the irradiation of photons at a particular wavelength [23]. Similarly, when plasmonic

• particle size from 50 to 4.98 nm. In another study, the size-dependent photothermal conversion efficiency of platinum nanomaterials was studied by Depciuch et al. for cancer therapy. Spherical platinum nanoparticles with diameters of 2 and 80 nm were studied regarding the photothermal activity in colon

• reduced graphene oxide (rGO), SERS imaging can be done along with photothermal therapy [84]. Recently, our group developed a multifunctional rGO–Au nanoscale architecture loaded with Raman dye and anticancer drugs for fluorescence/SERS imaging-guided breast cancer therapy. Under activation of a laser at

Antibody-conjugated nanoparticles for target-specific drug delivery of chemotherapeutics

• Mamta Kumari,
• Amitabha Acharya and
• Praveen Thaggikuppe Krishnamurthy

Beilstein J. Nanotechnol. 2023, 14, 912–926, doi:10.3762/bjnano.14.75

• improvement, further investigations are required. Moreover, extensive research is still required in the field of clinical safety of ACNPs to evolve a highly acceptable and beneficial delivery system for cancer theranosis. Future perspectives In cancer therapy, ACNPs have several advantages related to their

• , detection, and eradication of cancer cells and biomarkers, with great potential in theranostic applications. Despite these advantages, the design and fabrication of targeted NPs for cancer therapy is still very challenging regarding biocompatibility, pharmacokinetics, in vivo targeting efficacy, and cost

Nanotechnology – a robust tool for fighting the challenges of drug resistance in non-small cell lung cancer

• Filip Gorachinov,
• Fatima Mraiche,
• Diala Alhaj Moustafa,
• Ola Hishari,
• Yomna Ismail,
• Jensa Joseph,
• Maja Simonoska Crcarevska,
• Marija Glavas Dodov,
• Nikola Geskovski and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2023, 14, 240–261, doi:10.3762/bjnano.14.23

• siRNA in the downregulation of oncogenes offers numerous advantages in combinatorial lung cancer treatment for targeting mutations that contribute to the resistance to cancer therapy. Synthetic siRNA can be designed to inhibit any target gene expression and consequently prevent or decrease target

• contribute to cancer therapy resistance encouraged the therapeutic application of RNA interference as a powerful tool to fight resistant tumors. Knockdown of oncogenic genes involved in drug resistance combined with traditional therapy or molecularly targeted agents for subsequent tumor killing may alleviate

Facile preparation of Au- and BODIPY-grafted lipid nanoparticles for synergized photothermal therapy

• Yuran Wang,
• Xudong Li,
• Haijun Chen and
• Yu Gao

Beilstein J. Nanotechnol. 2022, 13, 1432–1444, doi:10.3762/bjnano.13.118

• specificity and minimal invasiveness, it has attracted a great deal of attention as complementary modality for conventional cancer therapy options [1]. Gold nanoparticles (AuNPs) can absorb light and generate heat from light absorption because of the surface plasmon resonance (SPR) phenomenon and the tunable

• delivery systems through van der Waals forces, hydrogen bonds, π–π stacking, or electrostatic or hydrophobic interactions [24]. Several BODIPYs have been reported to be loaded into liposomes for cancer therapy [25]. Therefore, we speculated that BODIPY can be associated with our previously reported