Elasticity, an often-overseen parameter in the development of nanoscale drug delivery systems

• Agnes-Valencia Weiss and
• Marc Schneider

Beilstein J. Nanotechnol. 2023, 14, 1149–1156, doi:10.3762/bjnano.14.95

• filled with poly(lactic-co-glycolic acid) (PLGA) cores of different sizes resulting in interfacial water layers with different thicknesses and therefore with tunable elasticity [38]. Semielastic particles whose Young’s moduli were around 50 mPa showed the fastest diffusion in mucus. However, harder

• particles showed better cellular uptake if no mucus layer was present. In contrast to this, the cellular uptake for semielastic particles was not significantly affected by the presence of a mucus layer [38]. Liposomes with PLGA cores were used by Yu et al. to increase the stiffness in combination with

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

• . In a two-step reaction, NHS/sulfo-NHS evades the intra- and intermolecular cross-linking of the antibodies as the antibodies have both amine and carboxyl groups [48]. Acharya et al. prepared rapamycin-loaded polymeric PLGA NPs and conjugated them with cetuximab using EDC/NHS cross-linking chemistry

• stable irreversible thioether linkages [55]. Swaminathan et al. used the maleimide conjugation technique to coat the surface of paclitaxel-loaded-PLGA NPs with anti-CD133 antibody. The antibody-conjugated NPs improved the intracellular uptake of paclitaxel as well as the targeting effectiveness of the

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

• , nanoparticle concentration, surface functionalization, and the type of polymers that can be processed. Keywords: ethyl cellulose; nanoemulsions; nanomedicine; phase inversion composition (PIC) method; PLGA; polymer nanoparticles; polyuria; polyurethane; surfactants; Review 1 Introduction The field of

• diameter dE = 50 ± 12 nm (estimated by cryo-TEM), whereas the diameter of the derived PLGA nanoparticles (dP) was 25 ± 7 nm as estimated from TEM [24], which gives a dP/dE ratio of 0.5. Higher dP/dE ratios were found by dynamic light scattering, especially at low polymer concentrations (note that the

• . Conventional emulsification methods generally yield nanoparticles with sizes larger than those described above. For example, emulsions prepared with poly(vinylalcohol) (PVA) as stabilizer produce PLGA polymer microparticles with a size of several tens of micrometers after extraction or evaporation of the

Recent progress in cancer cell membrane-based nanoparticles for biomedical applications

• Qixiong Lin,
• Yueyou Peng,
• Yanyan Wen,
• Xiaoqiong Li,
• Donglian Du,
• Weibin Dai,
• Wei Tian and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2023, 14, 262–279, doi:10.3762/bjnano.14.24

• , cancer cell membrane-encapsulated NPs can achieve better targeting toward tumors. Fang et al. coated poly (lactic-co-glycolic acid) (PLGA) NPs with the MDA-MB-435 human breast cancer cell membrane. The encapsulated biomimetic NPs exhibited a stronger affinity for cultured MDA-MB-435 cells in vitro than

• storage time than bare NPs because of the higher colloidal stability of the prepared colloidal particles [53]. In one study, liver cancer cell membrane-encapsulated PLGA NPs maintained a stable size in water and PBS for a long time, while bare PLGA NPs progressively grew larger (Figure 4B) [31]. 3

• ]. A biomimetic particle model using PLGA NPs as a carrier for the anticancer drug doxorubicin (Dox) encapsulated by the HepG2 liver cancer cell membrane was designed for the treatment of HCC [31]. The HepG2 cell membrane-encapsulated NPs exhibited superior antitumor effects compared to bare NPs and

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

• example of biomimetic NPs was described designed by Wang and co-workers. They used the natural tropism of mouse bone marrow mesenchymal cells (MSCs) for lung tumors for improved targeting of docetaxel (DTX) NPs (DTX-loaded polylactide-co-glycolide-b-poly(ethylene glycol); PLGA-b-PEG) loaded into the MSCs

• . The authors used animal models to show predominant lung trapping of MSCs in both rabbit and monkey. In vitro experiments in A549 NSCLC cells pointed to the release of the DTX-loaded PLGA-b-PEG NPs from the MSCs and their subsequent internalization. Efficient internalization and tumor inhibition were

Orally administered docetaxel-loaded chitosan-decorated cationic PLGA nanoparticles for intestinal tumors: formulation, comprehensive in vitro characterization, and release kinetics

• Sedat Ünal,
• Osman Doğan and
• Yeşim Aktaş

Beilstein J. Nanotechnol. 2022, 13, 1393–1407, doi:10.3762/bjnano.13.115

• drug delivery system loaded with docetaxel (DCX) as an anticancer drug, using poly(lactic-co-glycolic acid) (PLGA) as nanoparticle material, and modified with chitosan (CS) to gain mucoadhesive properties. In this context, an innovative nanoparticle formulation that can protect orally administered DCX

• from GIT conditions and deliver the drug to the intestinal tumoral region by accumulating in mucus has been designed. For this purpose, DCX-PLGA nanoparticles (NPs) and CS/DCX-PLGA NPs were prepared, and their in vitro characteristics were elucidated. Nanoparticles around 250–300 nm were obtained. DCX

• -PLGA NPs had positive surface charge with CS coating. The formulations have the potential to deliver the encapsulated drug to the bowel according to the in vitro release studies in three different simulated GIT fluids for approximately 72 h. Mucin interaction and penetration into the artificial mucus

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

• ) [130], and poly(lactic-co-glycolic)acid (PLGA) [131] are widely investigated as microneedle materials. Among them, there are hydrogel-forming agents swelling upon the contact with interstitial fluid in the skin during microneedle application. These polymers include poly(ethylene glycol) diacrylate

• ], calcium sulfate and gelatin [135], gelatin and hydroxyapatite [136], and PLGA microparticles combined with PLA [137] are available in the scientific literature. Taking into consideration the shape and geometry of microneedles, they can be categorized as pyramids, cones, arrowheads, cylinders, bullets

• in PLGA-based nanoparticles by a water-in-oil-in-water double emulsion method. The nanoparticles were used to form microneedles in combination with various types of PVA. Then, after drying, a base layer made of an aqueous hydrogel was attached. It turned out that the MNs had adequate mechanical

Biomimetic chitosan with biocomposite nanomaterials for bone tissue repair and regeneration

• Se-Kwon Kim,
• Sesha Subramanian Murugan,
• Pandurang Appana Dalavi,
• Sebanti Gupta,
• Sukumaran Anil,
• Gi Hun Seong and
• Jayachandran Venkatesan

Beilstein J. Nanotechnol. 2022, 13, 1051–1067, doi:10.3762/bjnano.13.92

• . Different kinds of polymeric materials have been utilized including chitosan, alginate, fucoidan, carrageenan, and ulvan from natural polymeric materials. Polycaprolactone (PCL), poly ᴅ,ʟ-lactic-co-glycolic acid (PLGA), and polylactic acid (PLA) have been extensively studied with hydroxyapatite to develop

• fabrication of scaffolds for cartilage tissue engineering applications. The 2 cm × 2 cm PLGA electrospun nanofibers were prepared by electrospinning which incorporated those with hydroxybutyl chitosan hydrogels. The polycaprolactone scaffold was 3D printed and reinforced with hydrogel scaffolds to mimic the

Gelatin nanoparticles with tunable mechanical properties: effect of crosslinking time and loading

• Agnes-Valencia Weiss,
• Daniel Schorr,
• Julia K. Metz,
• Metin Yildirim,
• Saeed Ahmad Khan and
• Marc Schneider

Beilstein J. Nanotechnol. 2022, 13, 778–787, doi:10.3762/bjnano.13.68

• . demonstrated the impact of the measurement setup for polymeric nanoparticles [4]. Young’s moduli obtained by measurements conducted on bulk materials and nanoparticles composed of PLA and PLGA vary significantly from each other. Furthermore, they showed the impact of measurements in water and at physiological

Fabrication and testing of polymer microneedles for transdermal drug delivery

• Vahid Ebrahiminejad,
• Zahra Faraji Rad,
• Philip D. Prewett and
• Graham J. Davies

Beilstein J. Nanotechnol. 2022, 13, 629–640, doi:10.3762/bjnano.13.55

• (PLGA) MNs with a similar base diameter (200 μm) and lengths (700–1500 μm) [22]. Simulation and experimental investigation on MN insertion force To investigate the insertion force and failure modes of MN arrays into the skin, the insertion of a single MN was simulated using FEA software. Figure 6a

Stimuli-responsive polypeptide nanogels for trypsin inhibition

• Petr Šálek,
• Jana Dvořáková,
• Sviatoslav Hladysh,
• Diana Oleshchuk,
• Ewa Pavlova,
• Jan Kučka and
• Vladimír Proks

Beilstein J. Nanotechnol. 2022, 13, 538–548, doi:10.3762/bjnano.13.45

• ) (PLGA) nanoparticles loaded with AAT were successfully manufactured and AAT release profiles from the nanoparticles were investigated [21][22]. In our previous studies, we investigated and described in detail the process of nanogelation from Nα-ʟ-lysine-grafted α,β-poly[(2-propyne)-ᴅ,ʟ-aspartamide-ran

• studies using PLGA particles as delivery system for AAT [21][22]. However, the PLGA particles did not exhibit any undesired entrapment of AAT as the polypeptide nanogels did. In contrast, our polypeptide nanogels are more advantageous due to the fact that they have a more favorable size, are soft, 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

• ) (PLGA) microspheres coated with TGF-β3 loaded heparin/poly(ʟ-lysine) NPs showed extended growth factor release for 28 days and were found to be excellent structures for cell adhesion and chondrogenic differentiation [27]. Apart from serving as cell adhesion platforms and growth factor supplements

• , microsphere structures can be independently used as carriers for the delivery of drugs and bioactive molecules to repair cartilage defects. The sustained release of PTH (1-34) from PLGA microspheres improved papain-induced defects in a rat model of OA and retained the bioactivity of the released peptide up to

• 19 days [28]. In another study, researchers developed PLGA-based microspheres to control the release of rapamycin in the joint [29]. The microspheres provided sustained and controlled release of rapamycin for several weeks, retained drug potency, and prevented OA-like changes in chondrocytes cultured

Effects of drug concentration and PLGA addition on the properties of electrospun ampicillin trihydrate-loaded PLA nanofibers

• Tuğba Eren Böncü and
• Nurten Ozdemir

Beilstein J. Nanotechnol. 2022, 13, 245–254, doi:10.3762/bjnano.13.19

• produce ampicillin trihydrate-loaded poly(lactic acid) (PLA) and PLA/poly(lactic-co-glycolic acid) (PLA/PLGA) polymeric nanofibers via electrospinning using 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as the solvent for local application in tissue engineering. The effects of ampicillin trihydrate

• concentration (4–12%) and addition of PLGA (20–80%) on the spinnability of the solutions, morphology, average nanofiber diameter, encapsulation efficiency, drug release, and mechanical properties of PLA and PLA/PLGA nanofibers were examined. All nanofibers were bead-free and uniform. They had favorable

• and controlled drug release for ten days was obtained with nanofibers containing 8% of drug. Thus, the ideal drug concentration was determined to be 8%. Nanofibers containing PLA/PLGA had a larger diameter than those including PLA. In addition, both the strength and elongation of nanofibers decreased

Engineered titania nanomaterials in advanced clinical applications

• Padmavati Sahare,
• Paulina Govea Alvarez,
• Juan Manual Sanchez Yanez,
• Gabriel Luna-Bárcenas,
• Samik Chakraborty,
• Sujay Paul and
• Miriam Estevez

Beilstein J. Nanotechnol. 2022, 13, 201–218, doi:10.3762/bjnano.13.15

• contributes to hydroxyapatite (HA) formation and bone matrix mineralization [71]. Likewise, nanophase titania/poly(lactic-co-glycolic acid) (PLGA) composites have been designed that showed greater osteoblast adhesion compared to plain PLGA [72]. In vivo tissue engineering (TE) holds tremendous potential in

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

• -loaded polymeric (PNP with PLGA) and lipid nanoparticles (SLN with hydrogenated coco-glycerides and poloxamer 188). They reported greater stability at 135 days (>90% retention), lower average particle size (127.10 ± 11.30 nm), and higher EE% (90.49 ± 1.20%) in CUR-SL, as compared to CUR-PNP (338.20

• inhibiting nitric oxide in cancer cells [14]. Dev et al. [142] reported that CUR-loaded BSA nanoparticles (6 µM) exposed to blue LED light inhibited the growth of glioblastoma stem cells better than F-CUR, which was attributed to an improved sustained intracellular release of CUR. Curcumin-loaded PLGA [poly

An overview of microneedle applications, materials, and fabrication methods

• Zahra Faraji Rad,
• Philip D. Prewett and
• Graham J. Davies

Beilstein J. Nanotechnol. 2021, 12, 1034–1046, doi:10.3762/bjnano.12.77

• microneedles of soluble poly(lactic-co-glycolic acid) (PLGA) and PLGA–polyvinylpyrrolidone (PLGA–PVP) layered combinations have been used to provide controlled drug delivery of bovine serum albumin (BSA), rather than instantaneous release [60]. There are only a few published studies demonstrating the

• and sizes for a wide range of applications. Metals such as titanium [61][62], stainless steel [58][63][64], silicon [65][66][67], ceramics [68][69], biodegradable polymers such as polylactic acid (PLA) [70], PLGA [71], and polyglycolic acid (PGA) [72], and non-degradable polymers such as

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

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

• with higher turnover rates [33]. The authors used alendronate as a surface-exposed ligand for directing bortezomib-loaded nanoparticles consisting of poly(ᴅ,ʟ-lactic-co-glycolic acid) (PLGA) and poly(ethylene glycol) (PEG) to the bone microenvironment, which resulted in a 9.6-fold increase of bone

• localization of the functionalized nanoparticles relative to the non-functionalized nanoparticles. Additionally, the loaded PLGA–PEG–alendronate nanoparticles demonstrated satisfactory results in myeloma growth inhibition and overall survival of the murine models. Considering the toxicity of bortezomib

Differences in surface chemistry of iron oxide nanoparticles result in different routes of internalization

• Barbora Svitkova,
• Vlasta Zavisova,
• Veronika Nemethova,
• Martina Koneracka,
• Miroslava Kretova,
• Filip Razga,
• Monika Ursinyova and
• Alena Gabelova

Beilstein J. Nanotechnol. 2021, 12, 270–281, doi:10.3762/bjnano.12.22

• , essential for the interpretation of their biological effects, including cellular uptake [43]. Nevertheless, PEG-SO-MNPs were more efficiently internalized into A549 cells than BSA-SO-MNPs. Interestingly, the magnetic nanospheres (PEG-SO-MNPs coated with polylactic-co-glycolic acid, PLGA) were taken up by

Key for crossing the BBB with nanoparticles: the rational design

• Sonia M. Lombardo,
• Marc Schneider,
• Akif E. Türeli and
• Nazende Günday Türeli

Beilstein J. Nanotechnol. 2020, 11, 866–883, doi:10.3762/bjnano.11.72

• polymeric nanoparticles prepared with PBCA and polymers from the poly(ethylene) family such as poly(lactic acid) (PLA) and poly(lactic-co-glycolic acid) (PLGA) [25][26]. Liposomes and other lipidic nanoparticles have also been reported as able to pass the BBB [27], as well as protein-based nanoparticles

• were observed for PLGA nanoparticles stabilized with PS80 or P188. PLGA nanoparticles loaded with either loperamide or doxorubicin were coated with PS80 or P188 and tested in vivo in rodents [56]. In both cases, P188-coated PLGA nanoparticles showed a higher efficacy than PS80-coated nanoparticles, but

• both formulations were able to cross the BBB and deliver their cargo. On the other hand, in another study, coumarin-6-loaded PLGA nanoparticles coated with either chitosan or PS80 showed a better crossing ability than P188-coated nanoparticles [57]. This result seems to be in accordance with the

Rational design of block copolymer self-assemblies in photodynamic therapy

• Maxime Demazeau,
• Laure Gibot,
• Anne-Françoise Mingotaud,
• Patricia Vicendo,
• Clément Roux and
• Barbara Lonetti

Beilstein J. Nanotechnol. 2020, 11, 180–212, doi:10.3762/bjnano.11.15

Microfluidics as tool to prepare size-tunable PLGA nanoparticles with high curcumin encapsulation for efficient mucus penetration

• Nashrawan Lababidi,
• Valentin Sigal,
• Aljoscha Koenneke,
• Konrad Schwarzkopf,
• Andreas Manz and
• Marc Schneider

Beilstein J. Nanotechnol. 2019, 10, 2280–2293, doi:10.3762/bjnano.10.220

• mucus. Drug carrier systems such as nanoparticles (NPs) require proper surface chemistry and small size to ensure their permeability through the hydrogel-like systems. We have employed a microfluidic system to fabricate poly(lactic-co-glycolic acid) (PLGA) nanoparticles coated with a muco-penetrating

• was loaded (EE% of ≈68%) very efficiently into the nanoparticles. Finally, the permeability of muco-penetrating PLGA NPs through pulmonary human mucus was assessed; small NPs with a diameter of less than 100 nm showed fast permeation, underlining the potential of microfluidics for such pharmaceutical

• applications. Keywords: curcumin; human pulmonary mucus; microfluidics; muco-penetrating nanoparticles; nanomedicine; permeability; PLGA nanoparticles; Introduction In the last decades, the application of nanotechnology in medicine has gained significant attention, especially in the biomedical field for

Incorporation of doxorubicin in different polymer nanoparticles and their anticancer activity

• Sebastian Pieper,
• Hannah Onafuye,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Martin Michaelis and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 2062–2072, doi:10.3762/bjnano.10.201

• . To investigate whether easy-to-prepare nanoparticles made of well-tolerated polymers may circumvent transporter-mediated drug efflux, we prepared poly(lactic-co-glycolic acid) (PLGA), polylactic acid (PLA), and PEGylated PLGA (PLGA-PEG) nanoparticles loaded with the ABCB1 substrate doxorubicin by

• solvent displacement and emulsion diffusion approaches and assessed their anticancer efficiency in neuroblastoma cells, including ABCB1-expressing cell lines, in comparison to doxorubicin solution. Results: The resulting nanoparticles covered a size range between 73 and 246 nm. PLGA-PEG nanoparticle

• preparation by solvent displacement led to the smallest nanoparticles. In PLGA nanoparticles, the drug load could be optimised using solvent displacement at pH 7 reaching 53 µg doxorubicin/mg nanoparticle. These PLGA nanoparticles displayed sustained doxorubicin release kinetics compared to the more burst

Microfluidic manufacturing of different niosomes nanoparticles for curcumin encapsulation: Physical characteristics, encapsulation efficacy, and drug release

• Mohammad A. Obeid,
• Ibrahim Khadra,
• Abdullah Albaloushi,
• Margaret Mullin,
• Hanin Alyamani and
• Valerie A. Ferro

Beilstein J. Nanotechnol. 2019, 10, 1826–1832, doi:10.3762/bjnano.10.177

• containing the polyanion sodium hyaluronate [8]. Ozeki et al., prepared a curcumin-loaded PEGylated PLGA through microfluidic mixing and achieved an EE of around 50% [20]. Here, high EE of around 60% was achieved using niosomes nanoparticles composed of T85 as a non-ionic surfactant. The encapsulation

Doxorubicin-loaded human serum albumin nanoparticles overcome transporter-mediated drug resistance in drug-adapted cancer cells

• Hannah Onafuye,
• Sebastian Pieper,
• Dennis Mulac,
• Jindrich Cinatl Jr.,
• Mark N. Wass,
• Klaus Langer and
• Martin Michaelis

Beilstein J. Nanotechnol. 2019, 10, 1707–1715, doi:10.3762/bjnano.10.166

• bind to doxorubicin via its amino group. Notably, the results differ from a recent similar study in which nanoparticles prepared from poly(lactic-co-glycolic acid) (PLGA) or polylactic acid (PLA), two other biodegradable materials approved by the FDA and EMA for human use [27][28], did not bypass ABCB1