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

• ][24]. Thus, using IR780 in our NPs would bring advantages for local imaging and treatment. Chemotherapy medications assist in inhibiting the development of tumors. Chemotherapeutic agents such as doxorubicin attach to chromosomes and inhibit DNA replication, while paclitaxel depolymerizes the

• cytoskeleton and chlorambucil (CHL) inhibits DNA synthesis. These drugs can be encapsulated inside nanoparticles for administration to increase the stability of the medication in circulation and therapeutic efficacy. For example, doxorubicin can be inserted into liposomes and paclitaxel attaches to the protein

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

• 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

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

• ]. This biomimetic strategy reduces the presence of the drug in normal tissues and clearance from the body, which will facilitate precision therapy and reduce the cytotoxicity of the drug to normal tissues. Similarly, as a commonly used chemotherapeutic drug, paclitaxel also faces many limiting problems

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

Systematic studies into uniform synthetic protein nanoparticles

• Nahal Habibi,
• Ava Mauser,
• Jeffery E. Raymond and
• Joerg Lahann

Beilstein J. Nanotechnol. 2022, 13, 274–283, doi:10.3762/bjnano.13.22

• molecules [7] and has been shown to be an attractive vehicle for hydrophobic drugs in several clinical and preclinical applications [8]. This feature is highlighted in the success of AbraxaneTM, a nanoparticle albumin bound (nab) technology to delivery paclitaxel – a hydrophobic cancer therapeutic

• . Paclitaxel was traditionally formulated through solubilization with harsh solvents, which led to adverse side effects and special administration instrumentation [9]. While AbraxaneTM was first FDA-approved for the treatment of metastatic breast cancer, it has since been investigated for other cancers

• , particularly as a combination therapy [10]. To leverage the endogenous properties of albumin, nab technology uses a high-pressure manufacturing process to force hydrophobic drugs into the internal hydrophobic pockets of human serum albumin (HSA) [11]. This leads to the formation of albumin-bound, paclitaxel

Biocompatibility and cytotoxicity in vitro of surface-functionalized drug-loaded spinel ferrite nanoparticles

• Sadaf Mushtaq,
• Khuram Shahzad,
• Tariq Saeed,
• Anwar Ul-Hamid,
• Bilal Haider Abbasi,
• Nafees Ahmad,
• Waqas Khalid,
• Muhammad Atif,
• Zulqurnain Ali and
• Rashda Abbasi

Beilstein J. Nanotechnol. 2021, 12, 1339–1364, doi:10.3762/bjnano.12.99

• efflux chemotherapeutic drugs, a phenomenon known as MDR. P-glycoprotein belongs to the ABCB1 family of ABC proteins and is involved in the efflux of doxorubicin, paclitaxel, vincristine, rhodamine, and etoposide [63]. Conversely, multidrug resistance-associated protein 1 (MRP1) is a member of the ABCC1

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

• %) [2]. The most commonly used treatments involve chemotherapy, surgery, or a combination of both. Chemotherapy is based on the use of molecules such as doxorubicin, paclitaxel, cisplatin, and some proteins and peptides that induce cell death [3]. Conventional or low molecular weight chemotherapeutics

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

• decreased without enhancing the risk of skin damage [131]. It has been established that ADV-mediated delivery of several chemotherapeutic drugs, including DOX [132], paclitaxel [133], and chlorambucil, could be achieved when loaded into PFC droplets [134]. The NDs could be successfully accumulated in a

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

• developed E-selectin-targeted porous silicon particles with capabilities for selective uptake to the BM [35]. The authors formulated a multistage carrier composed of porous silica microparticles that encapsulate nanoscale paclitaxel-loaded liposomes. The porous silica particles were decorated with E

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

• upregulated in many cancer types [56] aids the vesicle formation, facilitating the accumulation of albumin in the tumor mass [57]. This phenomenon forms the basis of Abraxane, a 130 nm paclitaxel-bound albumin nanodrug [58]. There is, however, no evidence that albondin is expressed on tumor cells; in contrast

Electrokinetic characterization of synthetic protein nanoparticles

• Daniel F. Quevedo,
• Cody J. Lentz,
• Adriana Coll de Peña,
• Yazmin Hernandez,
• Nahal Habibi,
• Rikako Miki,
• Joerg Lahann and
• Blanca H. Lapizco-Encinas

Beilstein J. Nanotechnol. 2020, 11, 1556–1567, doi:10.3762/bjnano.11.138

• vaccines [5][6]. Significant advances in self-assembled PNPs via protein engineering techniques have also been observed [7][8]. PNPs have successfully reached the clinic with nab-paclitaxel (Abraxane®), a PNP made of human serum albumin, which is being used for the treatment of metastatic breast cancer

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

• the survival time of mice when loaded with paclitaxel. Thus, this formulation could be a promising drug delivery system for antitumor therapy. Solid lipid nanoparticles: Solid lipid nanoparticles (SLNs) are particles with a solid lipid core at room and body temperature [27]. SLNs can be prepared with

Multilayer capsules made of weak polyelectrolytes: a review on the preparation, functionalization and applications in drug delivery

• Varsha Sharma and
• Anandhakumar Sundaramurthy

Beilstein J. Nanotechnol. 2020, 11, 508–532, doi:10.3762/bjnano.11.41

• drug-loaded PVPAlk capsules were even shown to overcome multidrug resistance with Dox and paclitaxel against LIM1899 colorectal cancer cells [98]. A new kind of dual (pH and redox) responsive, charge shifting click capsules based on poly(2-diisopropylaminoethyl methacrylate) (PDPA) were also fabricated

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

• ]. Once the PS has been chosen, the PS/vector affinity can be tuned by adjusting the polymer structure, introducing additional functional groups that are able to interact with the PS. This approach by itself is not new and Kataoka et al. used this strategy in 2005 to improve the loading of paclitaxel in

Bombesin receptor-targeted liposomes for enhanced delivery to lung cancer cells

• Mohammad J. Akbar,
• Pâmela C. Lukasewicz Ferreira,
• Melania Giorgetti,
• Leanne Stokes and
• Christopher J. Morris

Beilstein J. Nanotechnol. 2019, 10, 2553–2562, doi:10.3762/bjnano.10.246

• ]. In the lung cancer field, cisplatin formulated as a pegylated liposomal formulation (Lipoplatin®) has delivered comparable antitumour response against non-small cell lung cancer tumours with reduced side effects when delivered in combination with paclitaxel compared to when cisplatin and paclitaxel

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

• degradation, and sustain therapeutic drug concentrations due to prolonged/controlled drug release. In addition, nanoparticles can be used to administer poorly soluble agents, as demonstrated for nab-paclitaxel, a HSA nanoparticle-based paclitaxel preparation approved for the treatment of different forms of

Synthesis and potent cytotoxic activity of a novel diosgenin derivative and its phytosomes against lung cancer cells

• Liang Xu,
• Dekang Xu,
• Ziying Li,
• Yu Gao and
• Haijun Chen

Beilstein J. Nanotechnol. 2019, 10, 1933–1942, doi:10.3762/bjnano.10.189

• antiproliferative activity against HeLa cells, which is close to that of the clinical anticancer agent paclitaxel [14]. These successful examples demonstrated that the steroidal structure of Di is promising for the discovery of new anticancer drugs. Liposomes that usually consist of phospholipids and are stabilized

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

• -mediated drug efflux [29]. Differences in the mode of uptake and cellular distribution of the nanoparticles from different materials may be responsible for these discrepancies. HSA nanoparticles may be internalised upon interaction with cellular albumin receptors [30][31]. Notably, nab-paclitaxel, an HSA

• nanoparticle-based preparation of paclitaxel (another ABCB1 substrate [21]), which is approved for the treatment of different forms of cancer [32], had previously been shown not to avoid ABCB1-mediated drug efflux [33]. However, nab-paclitaxel is not produced by the use of cross-linkers, and the interaction of

• paclitaxel with albumin may differ from that of doxorubicin. Hence, variations in drug binding and drug release kinetics may be responsible for this difference. Despite the prominent role of ABCB1 as a drug resistance mechanism, attempts to exploit it as drug target have failed so far, despite the

Enhanced antineoplastic/therapeutic efficacy using 5-fluorouracil-loaded calcium phosphate nanoparticles

• Shanid Mohiyuddin,
• Saba Naqvi and
• Gopinath Packirisamy

Beilstein J. Nanotechnol. 2018, 9, 2499–2515, doi:10.3762/bjnano.9.233

• prior to arriving at the targeted site resulted in serious nonspecific cytotoxicity [4]. Alternative drug delivery strategies using inorganic nanoparticles have also been applied. A magneto-electric nanoparticle (MEN) system was reported as a controlled drug delivery platform for the drug paclitaxel in

Atomic-level characterization and cilostazol affinity of poly(lactic acid) nanoparticles conjugated with differentially charged hydrophilic molecules

• María Francisca Matus,
• Martín Ludueña,
• Cristian Vilos,
• Iván Palomo and
• Marcelo M. Mariscal

Beilstein J. Nanotechnol. 2018, 9, 1328–1338, doi:10.3762/bjnano.9.126

• descriptions using computational methodologies still are not totally addressed. Wang et al. [30] carried out dissipative particle dynamics (DPD) simulations to study the PEG–PLA–PEG/paclitaxel delivery system. The results showed a spherical micelle with the drug inside and polymer chains distributed on the

Review on nanoparticles and nanostructured materials: history, sources, toxicity and regulations

• Jaison Jeevanandam,
• Ahmed Barhoum,
• Yen S. Chan,
• Alain Dufresne and
• Michael K. Danquah

Beilstein J. Nanotechnol. 2018, 9, 1050–1074, doi:10.3762/bjnano.9.98

• powered by light on the market, representing the first major commercial use of dye-sensitized solar cells. In 2005, Abraxane™, which is a human serum albumin NP material containing paclitaxel, was manufactured, commercialized and released in the pharmaceutical market [41]. In 2014, there were about 1814

Nanoparticle delivery to metastatic breast cancer cells by nanoengineered mesenchymal stem cells

• Liga Saulite,
• Karlis Pleiko,
• Ineta Popena,
• Dominyka Dapkute,
• Ricardas Rotomskis and
• Una Riekstina

Beilstein J. Nanotechnol. 2018, 9, 321–332, doi:10.3762/bjnano.9.32

• to U251 glioma cells and induce cancer cell apoptosis [9]. Moreover, MSCs carrying poly(lactic-co-glycolic acid) (PLGA) NPs linked with paclitaxel selectively accumulate in an orthotopic A549 lung tumour model [2]. It has been reported that IFN-beta secreting MSCs could integrate into A375SM melanoma

Development of polycationic amphiphilic cyclodextrin nanoparticles for anticancer drug delivery

• Gamze Varan,
• Juan M. Benito,
• Carmen Ortiz Mellet and
• Erem Bilensoy

Beilstein J. Nanotechnol. 2017, 8, 1457–1468, doi:10.3762/bjnano.8.145

• , Spain Department of Organic Chemistry, University of Sevilla, C/ Prof García Gonzalez 1, Sevilla, 41012, Spain Department of Pharmaceutical Technology, Faculty of Pharmacy, Hacettepe University, Ankara, 06100, Turkey 10.3762/bjnano.8.145 Abstract Background: Paclitaxel is a potent anticancer drug that

• is effective against a wide spectrum of cancers. To overcome its bioavailability problems arising from very poor aqueous solubility and tendency to recrystallize upon dilution, paclitaxel is commercially formulated with co-solvents such as Cremophor EL® that are known to cause serious side effects

• agents for gene delivery in the form of nanoplexes. In this study, the potential of polycationic, amphiphilic cyclodextrin nanoparticles were evaluated in comparison to non-ionic amphiphilic cyclodextrins and core–shell type cyclodextrin nanoparticles for paclitaxel delivery to breast tumors. Pre

Cationic PEGylated polycaprolactone nanoparticles carrying post-operation docetaxel for glioma treatment

• Cem Varan and
• Erem Bilensoy

Beilstein J. Nanotechnol. 2017, 8, 1446–1456, doi:10.3762/bjnano.8.144

• , facilitating chemotherapy administration to prevent recurrence of the tumor at the time of tumor tissue removal by surgical operation. Among the anticancer drugs that are used in clinics, the taxane family of drugs such as paclitaxel and docetaxel are known to be highly effective against a variety of cancer

• -insoluble drugs from HpC films was examined by different study groups and the release profile was shown to be completed within approximately 10 h [71][72][73]. In another study regarding the release of paclitaxel (which is another member of taxane class, such as docetaxel, released from nanocomposite film

Carbon nanomaterials sensitize prostate cancer cells to docetaxel and mitomycin C via induction of apoptosis and inhibition of proliferation

• Kati Erdmann,
• Jessica Ringel,
• Silke Hampel,
• Manfred P. Wirth and
• Susanne Fuessel

Beilstein J. Nanotechnol. 2017, 8, 1307–1317, doi:10.3762/bjnano.8.132

• have demonstrated that carbon nanomaterials can also act as anti-tumor agents themselves and sensitize cancer cells to cytotoxic drugs such as etoposide [23][24][26], dexamethasone [23], paclitaxel [25] and CDDP [16]. In accordance, we have previously shown that CNFs and multiwalled CNTs could enhance

• –DTX (cell colony formation), CNFs–MMC (cell death rate) and CNFs–CP (cell death rate), respectively (Table 3). Furthermore, other studies have also demonstrated that single-walled CNTs can augment the effectiveness of cytotoxic drugs such as etoposide and paclitaxel via enhanced apoptosis [24][25][26