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

• )) targeting solid tumours [66]. Triblock copolymers comprising poly(2-ethyl-2-oxazoline) (PEtOx), poly(2-n-propyl-2-oxazoline) (PnPrOx), and PLL (Mw = 6.9 kDa, degree of polymerization (DP) = 42) segments allowed for the formation of compartmentalised micelles bearing a hydrophilic PEtOx shell, a

• crucial role in gene silencing since it enabled the formation of (Luc-ASO-HE12):PEI–DNA micelles, which provided greater stability and protection of antisense nucleotides. This resulted in enhanced cell uptake and transfection activity when compared to free ASO and Luc-ASO-(HE-HEG)6 complexes

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

Nanoarchitectonics with cetrimonium bromide on metal nanoparticles for linker-free detection of toxic metal ions and catalytic degradation of 4-nitrophenol

• Akash Kumar and
• Raja Gopal Rayavarapu

Beilstein J. Nanotechnol. 2024, 15, 1312–1332, doi:10.3762/bjnano.15.106

• (5–50 µL) results in the controlled desorption of CTAB from the metal surface. A recent study demonstrated the ability of NaOH to interfere with CTAB micelles, where the pH value played a key role [33]. Optimized conditions enabled the linker-free sensing of heavy metal ions (Figure 1c

• plasmons due to the easy desorption of CTAB in the presence of NaOH, which is not observed in the case of small gold nanorods and nanospheres. The CTAB is tightly packed on short nanorods and nanospheres [43]. It was reported that NaOH significantly alters the micelles of quaternary ammonium surfactants

• CTAB micelles without hampering the physicochemical properties of the synthesized nanoparticles. This weakening of CTAB solves the persistent problem of surface modification or the use of linker molecules with CTAB-capped nanoparticles for sensing applications. In addition, the nanorod size might be

Synthesis, characterization and anticancer effect of doxorubicin-loaded dual stimuli-responsive smart nanopolymers

• Ömür Acet,
• Pavel Kirsanov,
• Burcu Önal Acet,
• Inessa Halets-Bui,
• Dzmitry Shcharbin,
• Şeyda Ceylan Cömert and
• Mehmet Odabaşı

Beilstein J. Nanotechnol. 2024, 15, 1189–1196, doi:10.3762/bjnano.15.96

• than free DOX. To date, several types of nanoparticles, such as liposomes, micelles, and metal-organic frameworks, have been studied to encapsulate DOX to obtain effective and non-toxic drugs [7][8]. Great attention has been paid to nanoparticles because of their specific properties, such as small size

Recent updates in applications of nanomedicine for the treatment of hepatic fibrosis

• Damai Ria Setyawati,
• Fransiska Christydira Sekaringtyas,
• Riyona Desvy Pratiwi,
• A’liyatur Rosyidah,
• Rohimmahtunnissa Azhar,
• Nunik Gustini,
• Gita Syahputra,
• Idah Rosidah,
• Etik Mardliyati,
• Tarwadi and
• Sjaikhurrizal El Muttaqien

Beilstein J. Nanotechnol. 2024, 15, 1105–1116, doi:10.3762/bjnano.15.89

• , liver-targeted nanocarriers are needed to increase the drug concentration in the liver with minimum off-target effects. For this purpose, both passive and active targeting strategies of nanomedicine-based drug deliveries have been studied. Liposomes, micelles, solid lipid NPs, and gold NPs are examples

• as an absorption enhancer [51]. The therapeutic potential of curcumin using nanoformulations was reviewed by several researchers, summarizing recent curcumin encapsulation works on various NP platforms (liposomes, solid lipid NPs, micelles, and polymeric NPs) [52][53]. For example, polymeric

Gold nanomakura: nanoarchitectonics and their photothermal response in association with carrageenan hydrogels

• Nabojit Das,
• Vikas,
• Akash Kumar,
• Sanjeev Soni and
• Raja Gopal Rayavarapu

Beilstein J. Nanotechnol. 2024, 15, 678–693, doi:10.3762/bjnano.15.56

• well known to generate anisotropic nanomaterials. The mechanism mainly involves the arrangement of surfactant micelles which dictates anisotropy in nanoparticle during synthesis. A seed is a tiny crystal of ≈2–3 nm that initiates growth of a nanoparticle when introduced in a proper growth solution. The

• structures, micelles with longer carbon tail lengths form more compact bilayer structures and vice versa. Also, the density of mixed micellar structure of CTAB is higher and is followed by MTAB and DTAB, respectively; thus, resulting in the formation of AuNMs of different aspect ratios. The corroboration of

• DTAB-AuNM, respectively. Growth mechanism of gold nanomakura particles (AuNM). (a) AuNM surrounded by surfactant micelles; (b) growth facet of AuNM; and (c) stepwise growth mechanism during AuNM formation. (a) Seed-mediated synthesis of CTAB-capped AuNR. (b) Seedless synthesis of DTAB-capped AuNR. (c

Nanomedicines against Chagas disease: a critical review

• Maria Jose Morilla,
• Kajal Ghosal and
• Eder Lilia Romero

Beilstein J. Nanotechnol. 2024, 15, 333–349, doi:10.3762/bjnano.15.30

• be able to do it? The answer is more political than technical. A search conducted on PubMed (17 November 2023), employing the following keywords (articles make no distinction between treatment and diagnosis): “Chagas and liposomes”, “Chagas and nanoparticles”, “Chagas and micelles”, “cruzi and

• liposomes”, “cruzi and nanoparticles”, “cruzi and micelles”; “leishmania and liposomes”, “leishmania and nanoparticles”, “leishmania and micelles”; “malaria and liposomes”, “malaria and nanoparticles”, “malaria and micelles”, “plasmodium and liposomes”, “plasmodium and nanoparticles”, and “plasmodium and

• micelles”. In vitro performance of BNZ-based nanomedicines.a In vivo performance of oral BNZ-based nanomedicines.a In vivo performance of nanomedicines based on non-approved drugs.

Development and characterization of potential larvicidal nanoemulsions against Aedes aegypti

• Jonatas L. Duarte,
• Leonardo Delello Di Filippo,
• Anna Eliza Maciel de Faria Mota Oliveira,
• Rafael Miguel Sábio,
• Gabriel Davi Marena,
• Tais Maria Bauab,
• Cristiane Duque,
• Vincent Corbel and
• Marlus Chorilli

Beilstein J. Nanotechnol. 2024, 15, 104–114, doi:10.3762/bjnano.15.10

• oil–surfactant core–shell structure within the micelles. Consequently, a lower amount of monoterpenes is released into the surrounding medium [42]. Among the mathematical models used to study drug kinetics, the Korsmeyer–Peppas release model proved to be the most suitable for our formulations (Table 4

Curcumin-loaded nanostructured systems for treatment of leishmaniasis: a review

• Douglas Dourado,
• Thayse Silva Medeiros,
• Éverton do Nascimento Alencar,
• Edijane Matos Sales and
• Fábio Rocha Formiga

Beilstein J. Nanotechnol. 2024, 15, 37–50, doi:10.3762/bjnano.15.4

• systems [19], nanoparticles [20], nanoliposomes [21], micelles [22], and nanocrystals [23] have been utilized. These systems can promote (i) protection of the drug against degradation in physiological media, (ii) increase in drug solubility, and (iii) modification/targeting of the drug enabling transport

The steep road to nonviral nanomedicines: Frequent challenges and culprits in designing nanoparticles for gene therapy

• Yao Yao,
• Yeongun Ko,
• Grant Grasman,
• Jeffery E. Raymond and
• Joerg Lahann

Beilstein J. Nanotechnol. 2023, 14, 351–361, doi:10.3762/bjnano.14.30

• polymeric (e.g., core–shell micelles), oligomeric (e.g., lipid nanoparticles), or biomacromolecular (e.g., protein nanoparticles) components complicates matters only further by generating a higher-than-normal background through non-specific interactions with the assay media. In addition, a significant bias

Polymer nanoparticles from low-energy nanoemulsions for biomedical applications

• Santiago Grijalvo and
• Carlos Rodriguez-Abreu

Beilstein J. Nanotechnol. 2023, 14, 339–350, doi:10.3762/bjnano.14.29

• (non-adsorbed) surfactant can be in the form of micelles that coexist with the nanoemulsion droplets. The kinetics of surfactant adsorption during droplet formation, droplet coarsening, as well as uncertainties in the estimation of as could also explain the divergences between calculated and

• surface charge (ca. −11 mV). The drug encapsulation efficiencies were higher than 98%, although loadings were not enough to achieve therapeutic concentrations. The GAL release from the nanoparticles was slower than that from aqueous GAL solutions and surfactant micelles. Viabilities of HeLa and SH-SY5Y

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

• )-functionalized nanoporous silica particles loaded with a poly(ʟ-glutamic acid) pH-cleavable linker–doxorubicin conjugate, which self-assembles into NPs after its release from the iNPG [114]. Li et al. designed a multistage nanocarrier for NSCLC targeting, composed of icotinib-loaded amphiphilic chitosan micelles

Cyclodextrins as eminent constituents in nanoarchitectonics for drug delivery systems

• Makoto Komiyama

Beilstein J. Nanotechnol. 2023, 14, 218–232, doi:10.3762/bjnano.14.21

• enhances the hydrophobic interactions of the poly(N-isopropylacrylamide) segments, stabilizing the hydrogel. The anticancer drug DOX encapsulated in the hydrophobic core is slowly released through the dissolution of the hydrogel to micelles. By modifying β-CyD with both N-acetyl-ʟ-cysteine and arginine

Solvent-induced assembly of mono- and divalent silica nanoparticles

• Bin Liu,
• Etienne Duguet and
• Serge Ravaine

Beilstein J. Nanotechnol. 2023, 14, 52–60, doi:10.3762/bjnano.14.6

• with two patches functionalized with metal-coordination-based recognition units [20], and by co-assembly of block copolymer micelles and hard nanoparticles [21]. Particles with two patches located at opposite poles have been assembled into a Kagome lattice by hydrophobic interactions [22], into chains

• -controlled patch-to-particle size ratio (PPSR) into dimers, trimers, tetramers, and spherical micelles at a low incubation time in mixtures of tetrahydrofuran (THF) and ethanol [32]. Here, we extend the study to 1-PSN with smaller PPSR values and to the use of another poor solvent for the PS patch (i.e

• previous work on the assembly of 1-PSN with larger PPSR ranging from 0.69 to 1.54 in a THF/ethanol mixture has shown that colloids with a low aggregation number (e.g., dimers, trimers, tetramers, and spherical micelles) could be obtained at a low incubation time. Also, the higher the PPSR value, the more

Microneedle-based ocular drug delivery systems – recent advances and challenges

• Piotr Gadziński,
• Anna Froelich,
• Monika Wojtyłko,
• Antoni Białek,
• Julia Krysztofiak and
• Tomasz Osmałek

Beilstein J. Nanotechnol. 2022, 13, 1167–1184, doi:10.3762/bjnano.13.98

• introduced into systems whose purpose is to provide the expected concentration in the treated tissue for the desired time period. The most frequently studied and described are liposomes [60][61], micelles [60][62], microparticles [63][64][65], nanoparticles [66][67], micro- [68][69], and nanoemulsions [70

Antibacterial activity of a berberine nanoformulation

• Hue Thi Nguyen,
• Tuyet Nhung Pham,
• Anh-Tuan Le,
• Nguyen Thanh Thuy,
• Tran Quang Huy and
• Thuy Thi Thu Nguyen

Beilstein J. Nanotechnol. 2022, 13, 641–652, doi:10.3762/bjnano.13.56

• ), and it remains a challenge to increase drug loading. Besides, the high cost and the complexity of nanoformulation production narrow the accessibility [32]. Regarding dendrimers, micelles, and polymeric nanoparticles, there are also issues with long-term stability, low drug loading efficiency, and

Micro- and nanotechnology in biomedical engineering for cartilage tissue regeneration in osteoarthritis

• Zahra Nabizadeh,
• Mahmoud Nasrollahzadeh,
• Hamed Daemi,
• Mohamadreza Baghaban Eslaminejad,
• Ali Akbar Shabani,
• Mehdi Dadashpour,
• Majid Mirmohammadkhani and
• Davood Nasrabadi

Beilstein J. Nanotechnol. 2022, 13, 363–389, doi:10.3762/bjnano.13.31

• delivery [50], in vitro diagnosis [51], in vivo imaging [52], and TE purposes. Various NPs can be prepared in the form of liposomes, nanocapsules, micelles, dendrimers, and nanospheres based on their composition and method of preparation. Basically, NPs are designed to function as carriers for bioactive

Coordination-assembled myricetin nanoarchitectonics for sustainably scavenging free radicals

• Xiaoyan Ma,
• Haoning Gong,
• Kenji Ogino,
• Xuehai Yan and
• Ruirui Xing

Beilstein J. Nanotechnol. 2022, 13, 284–291, doi:10.3762/bjnano.13.23

• antioxidant peptides by proteases. The combination of liposomes or polymers with different payload materials has been reported, for example, PEG-modified liposomes loaded with resveratrol, layer-by-layer-coated gelatin nanoparticles, or Gelucire-based solid lipid and polymeric micelles [14][15][16][17][18][19

Photothermal ablation of murine melanomas by Fe₃O₄ nanoparticle clusters

• Xue Wang,
• Lili Xuan and
• Ying Pan

Beilstein J. Nanotechnol. 2022, 13, 255–264, doi:10.3762/bjnano.13.20

• micelles and the formation of Fe3O4 nanoparticle clusters, which were then coated with polyvinylpyrrolidone (PVP) to improve stability, biocompatibility and chemical features of the nanoparticles. Further SEM measurements revealed the as-formed Fe3O4 NPCs to be spherical and uniformly sized with an average

Use of nanosystems to improve the anticancer effects of curcumin

• Andrea M. Araya-Sibaja,
• Norma J. Salazar-López,
• Krissia Wilhelm Romero,
• José R. Vega-Baudrit,
• J. Abraham Domínguez-Avila,
• Carlos A. Velázquez Contreras,
• Ramón E. Robles-Zepeda,
• Mirtha Navarro-Hoyos and
• Gustavo A. González-Aguilar

Beilstein J. Nanotechnol. 2021, 12, 1047–1062, doi:10.3762/bjnano.12.78

• nanosystems. According to previous evidence, the use of nanosystems is highly flexible since it can be tailored for numerous applications with highly specific goals. Polymeric micelles and theranostics (a strategy that combines treatment and diagnostics) are two examples of such applications that are based on

Comprehensive review on ultrasound-responsive theranostic nanomaterials: mechanisms, structures and medical applications

• Sepand Tehrani Fateh,
• Lida Moradi,
• Elmira Kohan,
• Michael R. Hamblin and
• Amin Shiralizadeh Dezfuli

Beilstein J. Nanotechnol. 2021, 12, 808–862, doi:10.3762/bjnano.12.64

• , and sonoporation. These effects can result in the release of encapsulated drugs or genes at the site of interest as well as cell death and considerable image enhancement. The present review discusses US-responsive theranostic nanomaterials under the following categories: MBs, micelles, liposomes

• carrier. The imaging applications of these materials will also be discussed. These materials include nanocarrier formulations and nanostructured contrast agents, such as microbubbles (MBs), surfactant-based carriers (including micelles, NEs, and niosomes), polymer-based carriers (including gels

• less-discussed US-responsive nanomaterials in addition to the conventional nanomaterials (i.e., microbubbles, micelles, liposomes, and nanoemulsions) is another distinguishable feature of this review. Ultrasound-responsive nanomaterials are discussed in terms of their background, structure, preparation

Rapid controlled synthesis of gold–platinum nanorods with excellent photothermal properties under 808 nm excitation

• Jialin Wang,
• Qianqian Duan,
• Min Yang,
• Boye Zhang,
• Li Guo,
• Pengcui Li,
• Wendong Zhang and
• Shengbo Sang

Beilstein J. Nanotechnol. 2021, 12, 462–472, doi:10.3762/bjnano.12.37

• micelles were formed in the solution. PtCl42− is complexed with CTAB micelles and then gets reduced at the surface of AuNRs by ascorbic acid. During the reaction, a relatively obvious Pt shell formed gradually. In sharp contrast, in the presence of Ag+, it is apparent that Pt grows mainly at the tip of the

• , as shown in curve Au@Pt-3 and Au@Pt-4 in Figure 3a. We hypothesize that with the increase of K2PtCl4 content, the collision frequency between PtCl42−-CTAB micelles and AuNRs also increased, and eventually, Pt smoothly covers the surface of AuNRs and forms a thicker Pt coating. The absorption spectra

A review on nanostructured silver as a basic ingredient in medicine: physicochemical parameters and characterization

• Gabriel M. Misirli,
• Kishore Sridharan and
• Shirley M. P. Abrantes

Beilstein J. Nanotechnol. 2021, 12, 440–461, doi:10.3762/bjnano.12.36

• ]. Separation of AgNPs from Ag+: The cloud point extraction (CPE) technique was initiated by Goto et al. and it is based on the solubilization capacity and on the cloud point of nonionic surfactants [148]. At the cloud point, the instability observed in the micelles is promoted by the dehydration of the

• hydrophilic groups with consequent formation of giant micelles (cages) providing reduced water solubility (which defines the cloud point transition). It is exactly at this point that the AgNPs get surrounded by these non-ionic micelles and separated from the ionic silver (hydrophilic character) [149]. The

The impact of molecular tumor profiling on the design strategies for targeting myeloid leukemia and EGFR/CD44-positive solid tumors

• Nikola Geskovski,
• Nadica Matevska-Geshkovska,
• Simona Dimchevska Sazdovska,
• Marija Glavas Dodov,
• Kristina Mladenovska and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2021, 12, 375–401, doi:10.3762/bjnano.12.31

• the improvement of the overall therapeutic efficacy. A targeted NDDS for the co-delivery of ponatinib and SAR302503 (selective JAK2 inhibitor) for efficient CML treatment was developed by Mu and co-workers [47]. The authors employed alendronate-decorated PLA–PEG micelles for BM targeting. Both

• ponatinib and SAR302503 are hydrophobic drugs and were co-encapsulated inside the hydrophobic core of PEG–PLA micelles by solvent displacement nanoprecipitation. The results demonstrated that the targeted NDDS enabled a high availability of the drugs inside the BM, which is a prerequisite for overcoming the

A review on the green and sustainable synthesis of silver nanoparticles and one-dimensional silver nanostructures

• Sina Kaabipour and
• Shohreh Hemmati

Beilstein J. Nanotechnol. 2021, 12, 102–136, doi:10.3762/bjnano.12.9

• humidity [233]. The sol–gel process is associated with costly precursors, process longevity, and difficulties regarding reproducibility [234]. 2.2.2 Reverse-micelle process. The reverse micelle is another approach for the synthesis of AgNPs. Reverse micelles are produced from surfactants such as sucrose

• AgNPs in sodium dioctyl sulfosuccinate (AOT) reverse micelles using ascorbic acid as the reductant and obtained particles with an average size of 6 nm. Yang et al. [154] used sodium borohydride as the reductant and octadecylamine (ODA) as the solvent and produced AgNPs with an average size of 3.38 nm

• concentration inside the reverse micelles [235]. AOT-microemulsions have been the most common microemulsions for the preparation of micelles [152]. However, this method may result in the synthesis of AgNPs with weak surface plasmon characteristics due to a broad surface plasmon band [152]. 2.2.3 Chemical vapor