F127 Block Copolymer Research Articles

High efficacy of chloroquine-derived bile salts in Pluronic F127 micelles against blood-stage Plasmodium falciparum

Colloidal nanocarriers can play a key role in the efficacious delivery of drugs, including antimalarials. Here, we investigated the ability of polymeric micelles of the block copolymer F127 to act as nanovehicles for two organic salts derived from chloroquine and human bile acids, namely, chloroquinium cholate (iCQP1) and chloroquinium glycocholate (iCQP1g). We have previously reported the strong in vitro antiplasmodial activity of these salts, which displayed IC50 values of 13 and 15 nM against blood forms of Plasmodium falciparum, respectively. By deriving from amphiphilic lipids, iCQP1 and iCQP1g also enclose the ability to act as surface-active ionic liquids (SAILs). The micellization properties of neat F127 and of the F127/SAIL mixtures were initially investigated to gain physicochemical insight into the interaction between polymer and bioactive SAILs, resorting to differential scanning calorimetry, surface tension measurements and dynamic light scattering. Micelle formation by F127 is an endothermic process strongly temperature and concentration dependent. Interestingly, this process is significantly changed when the molar fraction of SAIL (xSAIL) in the F127/SAIL mixture is varied between 0.33 and 0.90. Both SAILs favor the formation of mixed micelles by decreasing the micellization temperature, and (observed only when for xSAIL = 0.33) by synergistically decreasing the cmc. Concomitantly, the micellar size is reduced from 18 to 13 nm as xSAIL is increased from 0.33 to 0.90. Crucially, in vitro assays show that when the SAILs are loaded into F127 polymeric micelles, their antiplasmodial efficacy is substantially enhanced, with a significant drop in IC50, especially for the iCQP1/F127 system. This opens new possibilities for the nanoformulations of antimalarial compounds.

Near infra-red absorbing Quinolizidine fused curcuminoid-BF2 chelate and its applications in photodynamic therapy using MCF-7 and A549 cells

Metal-free near-infrared absorbing photosensitizers (PS) have been considered promising candidates for photodynamic therapy. Curcumin, curcuminoid, and its derivatives have therapeutic values due to their anti-inflammatory, antifungal, and antiproliferative properties. Curcuminoid-BF2 chelates have also been studied as cell imaging probes, however, their applications in photodynamic therapy are rare. In this article, we describe the synthesis and therapeutic evaluation of quinolizidine fused curcuminoid-BF2 chelate (Quinolizidine CUR-BF2) containing an acid-sensitive group. This donor-acceptor-donor curcuminoid-BF2 derivative exhibits absorption and emission in the deep red region with an absorption band maximum of ∼647 nm and a weak emission band at approximately 713 nm. It is interesting to note that this derivative has a high molar extinction coefficient (164,655 M−1cm−1). Quinolizidine CUR-BF2 possesses intramolecular charge transfer properties, facilitating the production of singlet oxygen (1O2), which plays a crucial role in cell death. Additionally, Quinolizidine CUR-BF2 can enable the selective release of active ingredients in an acidic medium (pH 5). Furthermore, the nanoaggregates of PS were prepared by encapsulating Quinolizidine CUR-BF2 within Pluronic F127 block co-polymer for better water-dispersibility and enhanced cellular uptake. Dark cytotoxicity of nanoaggregates was found to be negligible, whereas they exhibited significant photoinduced cytotoxicity towards cancer cells (MCF-7 and A549) under irradiation of 635 nm light. Further, the cell death pathway using Quinolizidine CUR-BF2 nanoaggregates as PS is found to occur through apoptosis. Specifically, the present study deals with the successful preparation of Quinolizidine CUR-BF2 nanoaggregates for enhanced water-dispersibility and cellular uptake as well as the efficacy evaluation of developed nanoaggregates for photodynamic therapy.

Mixed Hyperbranched/Triblock Copolymer Micelle Assemblies: Physicochemical Properties and Potential for Drug Encapsulation

AbstractMixed micelles have numerous advantages while requiring little to no effort in preparation. This study aims to produce mixed micelle nanostructures from a linear triblock copolymer and a hyperbranched random copolymer, and is able to be loaded with the weakly water‐soluble drugs curcumin and indomethacin. Different preparation techniques are employed to produce mixed micelles comprised of Pluronic F127 block copolymer, and hyperbranched poly[(ethylene glycol) methyl ether methacrylate‐co‐lauryl methacrylate], H‐[P(OEGMA‐co‐LMA)], copolymer. Few studies have dabbled in these types of coassemblies, which provides insight into how structural differences of each copolymer can affect the formation of micelles. To determine the properties of the emerging nanostructures in aqueous environments, including their size, homogeneity, and surface charge, different physicochemical techniques are used, such as light scattering and spectroscopic methods. The results reveal that the copolymers combine, and spontaneously self‐assemble into mixed micelle‐like nanostructures in aqueous environments, whereas both systems of neat and drug‐loaded nanostructures exhibit desirable properties such as small average micelle hydrodynamic radii and low size polydispersity indices. The nanostructures that result from the effective encapsulation of curcumin exhibit outstanding stability over 169 days. The fluorescent qualities of curcumin persist after encapsulation, making the novel nanostructures excellent candidates for bioimaging applications.

UV-Accelerated Synthesis of Gold Nanoparticle-Pluronic Nanocomposites for X-ray Computed Tomography Contrast Enhancement.

Eco-friendly chemical methods using FDA-approved Pluronic F127 (PLU) block copolymer have garnered much attention for simultaneously forming and stabilizing Au nanoparticles (AuNPs). Given the remarkable properties of AuNPs for usage in various fields, especially in biomedicine, we performed a systematic study to synthesize AuNP-PLU nanocomposites under optimized conditions using UV irradiation for accelerating the reaction. The use of UV irradiation at 254 nm resulted in several advantages over the control method conducted under ambient light (control). The AuNP-PLU-UV nanocomposite was produced six times faster, lasting 10 min, and exhibited lower size dispersion than the control. A set of experimental techniques was applied to determine the structure and morphology of the produced nanocomposites as affected by the UV irradiation. The MTT assay was conducted to estimate IC50 values of AuNP-PLU-UV in NIH 3T3 mouse embryonic fibroblasts, and the results suggest that the sample is more compatible with cells than control samples. Afterward, in vivo maternal and fetal toxicity assays were performed in rats to evaluate the effect of AuNP-PLU-UV formulation during pregnancy. Under the tested conditions, the treatment was found to be safe for the mother and fetus. As a proof of concept or application, the synthesized Au:PLU were tested as contrast agents with an X-ray computed tomography scan (X-ray CT).

Mesostructured γ-Al2O3-Based Bifunctional Catalysts for Direct Synthesis of Dimethyl Ether from CO2

In this work, we propose two bifunctional nanocomposite catalysts based on acidic mesostructured γ-Al2O3 and a Cu/ZnO/ZrO2 redox phase. γ-Al2O3 was synthesized by an Evaporation-Induced Self-Assembly (EISA) method using two different templating agents (block copolymers Pluronic P123 and F127) and subsequently functionalized with the redox phase using an impregnation method modified with a self-combustion reaction. These nanocomposite catalysts and their corresponding mesostructured supports were characterized in terms of structural, textural, and morphological features as well as their acidic properties. The bifunctional catalysts were tested for the CO2-to-DME process, and their performances were compared with a physical mixture consisting of the most promising support as a dehydration catalyst together with the most common Cu-based commercial redox catalyst (CZA). The results highlight that the most appropriate Pluronic for the synthesis of γ-Al2O3 is P123; the use of this templating agent allows us to obtain a mesostructure with a smaller pore size and a higher number of acid sites. Furthermore, the corresponding composite catalyst shows a better dispersion of the redox phase and, consequently, a higher CO2 conversion. However, the incorporation of the redox phase into the porous structure of the acidic support (chemical mixing), favoring an intimate contact between the two phases, has detrimental effects on the dehydration performances due to the coverage of the acid sites with the redox nanophase. On the other hand, the strategy involving the physical mixing of the two phases, distinctly preserving the two catalytic functions, assures better performances.

Preparation of S self-doped porous carbon nanospheres as ORR catalysts derived from block copolymer grafted S group

In order to increase the activity and decrease the cost of oxygen reduction reaction (ORR) catalyst, S self-doped porous carbon nanospheres ORR catalyst was prepared by pyrolyzing the block copolymer F127 grafted with 3-mercapto-propanoicaci. The composition and microstructure were characterized and its electrochemical performance was also investigated in O2-saturated 0.1 M KOH solutions. The results showed that, among all the obtained samples, C-S-750 had a porous carbon nanosphere structure with the doped sulfur of 7.08 at % and a maximum specific surface area of 776.3 m2/g. The onset potential, half-wave potential and limiting current density of C-S-750 were 0.92 V (versus RHE) and 0.80 V (versus RHE) and 5.77 mA/cm2@0.45 V in O2-saturated 0.1 M KOH solution, respectively, which were close to that of commercial 20% Pt/C catalysts. This provides a new way to introduce and increase the doped heteroatom in metal-free ORR catalysts.

Grafting Poly(ethyleneimine) on Macroporous Core–Sheath Copolymer Beads with a Robust Framework for Stable CO2 Capture under Low-Temperature Regeneration

A macroporous organic adsorbent was designed and prepared using the template method, with acrylamide (AM) as the skeleton, glycidyl methacrylate (GMA) as the shell, and F-127 and Pluronic block copolymer (P123) as surfactants, and grafted with polyethyleneimine (PEI). Solid adsorbents were used for carbon dioxide capture. The effect of the AM/GMA mass ratio on the spherical morphology, through-hole structure, specific surface area, hardness, hydrophobicity, and thermal stability was comprehensively investigated, and the CO2 adsorption performance of the PEI-modified adsorbent was studied. Surface area and morphology characterization showed that after the introduction of GMA, the wall thickness and roughness increased, and the specific surface area and the mass of GMA first showed a positive correlation and then a negative correlation. In addition, the thermal stability was slightly reduced, and the hydrophobicity was greatly improved. The CO2 adsorption results revealed that the organic adsorbents exhibited higher adsorption capacity and faster adsorption kinetics than conventional CO2 capture materials, and their simple synthesis enables their industrial application. The study revealed that the preparation of PEI-modified adsorbents with a core–shell structure greatly improved thermal stability and selectivity. When the PEI loading was 50 wt %, the CO2 capacity of the core–shell microspheres reached 3.11 mmol·g–1 at 40 °C, and desorption can be completed at 85 °C. The proposed material has a good industrial application prospect and shows an excellent lifetime performance.

3D-printed surgical wound dressing for prolonged 5-fluorouracil delivery from pluronic blending composites

A direct drug delivery system of with the inhibition of multidrug resistance was developed in this study by the polymer mixing of Pluronic block copolymer F127, L121, polyethylene glycol (PEG), and polyvinyl alcohol (PVA). The polymer mixing was defined as Pluronic blending composites (PBCs) and optimized through adjusting the ratio of two different water-soluble homopolymers, PEG and PVA. The chemotherapeutic drugs of 5-fluorouracil (5-FU) were released from Pluronic blending composites nearly one month without continuous supplementary. Also, the effective ingredient of L121 inhibited multidrug resistance in human pancreatic cancer and caused the malfunction of the ATP binding cassette subfamily C (ABCC) transporter as evidenced by the flow cytometer studies. PBC-3 effectively suppresses the function of ABCC transporter up to 25 days. 5-FU are able to accumulate in the cancer cells of AsPC-1 and PANC-1 at a designated effective concentration. Then, a surgical dressing was prepared by 3D bio-printing technology with Pluronic blending composites cross-linked by sodium alginate. Results show that the surgical dressing of 24 layers with 10 mm × 10 mm would continuously release 5-FU in effective anticancer concentration for six days.

Impact of copper phthalocyanine structure on catalytic activity when incorporated into hierarchically porous carbon

A copper porphyrin and two copper phthalocyanine complexes were incorporated into a hierarchically porous carbon support formed by a sol-gel resorcinol-formaldehyde polymerization templated by F-127 block copolymer. The F127 self-organization leads to formation of mesostructure that on carbonization produces mesopores. Striking differences in catalytic activity for iodobenzene/imidazole cross coupling were observed between Alcian Blue-8gx (CuPc-8gx) (active) and copper phthalocyanine disulfonate (CuPc2S) (inactive). FTIR and EPR spectroscopy confirmed that phthalocyanine remained in the carbon after it was formed by heating to 500 °C, but that no complex survived heating to 800 °C. Electron microscopy (SEM and TEM) showed that the two dyes were differently distributed within the carbon support and found very different sizes of copper nanoparticles: 1.5 nm for CuPc-8gx and 86 nm for CuPc2S. Based on quenching of pyrene fluorescence by the two dyes it was concluded that CuPc-8gx was incorporated into F127 micelles. During polymerization the CuPc-8gx remained associated with F127 and so was incorporated into the polymer and subsequently the carbon. CuPc2S was not associated with F127 micelles, was not incorporated into the polymer and instead precipitated out during drying. This led to large CuPc2S nanoparticles, which resulted in very large copper nanoparticles with no catalytic activity.

Self-template synthesis of mesoporous vanadium oxide nanospheres with intrinsic peroxidase-like activity and high antibacterial performance

Mesoporous vanadium oxide nanospheres are a very promising nanozyme for antibacterial and chemical sensing. However, controllable synthesis of mesoporous vanadium oxide nanospheres with uniform structure and small diameter (<200 nm) remains challenging. Herein, mesoporous vanadium oxide nanospheres (MVONs) with a small, uniform and adjustable particle size (52–105 nm), large mesopore size (5.1–5.8 nm), and high specific surface area (up to 63.7 m2 g−1) are constructed via a self-template strategy using tannic acid, formaldehyde and vanadium compounds as a polymerizable ligand, cross-linking agent and metal source, respectively. The relationships between synthesis conditions and material nanostructure are systematically investigated. The particle size and peroxidase-like activity of MVONs can be easily changed by adding different amounts of Pluronic block copolymer F127. Owing to the mesoporous structure, high specific surface area and small particle size, MVONs can effectively convert H2O2 into extremely toxic reactive oxygen species, and further kill Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). This research establishes a universal, reliable method for synthesizing mesoporous vanadium oxide nanospheres, which might be used in catalysis, biosensors, and antibacterial treatment.

Kinetics-controlled regulation for homogeneous nucleation and growth of colloidal polymer and carbon nanospheres.

Size regulation of uniform polymer nanospheres (PNSs) and carbon nanospheres (CNSs) below 100 nm has been difficult and is limited by multiple factors, such as ongoing nucleation, Ostwald ripening, minimization of surface energy, and high viscosity during the nucleation and growth process. In this study, a kinetics-controlled regulation is reported for the synthesis of monodispersed PNSs and corresponding CNSs with adjustable size below 100 nm. During the synthesis of PNSs, three distinct stages including surface energy control, surface tension control and viscosity control have been observed, where the concentration of block copolymer F127 (CF127) plays a vital role in affecting the nucleation rate of PNSs and tunes the diffusion rate of monomers and migration of particles during the nucleation and growth process. As a consequence, the size of monodisperse CNSs can be customized from 100 nm down to 41 nm with PDI below 5%.

Selective Synthesis of Carbon Nanorings via Asymmetric Intramicellar Phase-Transition-Induced Tip-to-Tip Assembly

The selective synthesis of energetically less favorable ring-shaped nanostructures by liquid phase synthetic chemistry is a huge challenge. Herein, we report a precise synthesis of carbon nanorings with a well-defined morphology and tunable thickness based on asymmetric intramicellar phase-transition-induced tip-to-tip assembly via mixing hydrophobic long-chain octadecanol and block copolymer F127. This orientational self-assembly depends on the hydrophobicity difference of the intermediate’s surface, which triggers directional interactions that surpass the entropy cost of undesired connections and help assemble intermediates into defined ringlike structures. Based on a ringlike template, carbon nanorings with adjustable sizes can be attained by changing synthetic variables. More importantly, diverse units including crescentlike, podlike, and garlandlike nanostructures can also be created through controlling the kinetics of the self-assembly process. This discovery lays a solid foundation for the challenging construction of such a precise configuration on the nanoscale, which would not only promote fundamental studies but also pave the way for the development of advanced nanodevices with unique properties.

Tiny dexamethasone palmitate nanoparticles for intravitreal injection: Optimization and in vivo evaluation

Tiny nanoparticles of dexamethasone palmitate (DXP) were designed as transparent suspensions for intravitreal administration to treat age-related macular degeneration (AMD). The influence of three surfactants (PEG-40-stearate and Pluronic block copolymers F68 and F127) on nanoparticles size and stability was investigated and led to an optimal formulation based on Pluronic F127 stabilizing DXP nanoparticles. Size measurements and TEM revealed tiny nanoparticles (around 35 nm) with a low opacity, compatible with further intravitreal injection. X-Ray powder diffraction (XRPD) and transmission electronic microscopy (TEM) performed on freeze-dried samples showed that DXP nanoparticles were rather monodisperse and amorphous. The efficacy of DXP nanoparticles was assessed in vivo on pigmented rabbits with unilateral intravitreal injections. After breakdown of the blood-retinal barrier (BRB) induced by injection of rhVEGF165 with carrier protein, DXP nanoparticles induced a restoration of the BRB 1 month after their intravitreal injection. However, their efficacy was limited in time most probably by clearance of DXP nanoparticles after 2 months due to their small size.

Antibiotic Cross-linked Micelles with Reduced Toxicity for Multidrug-Resistant Bacterial Sepsis Treatment.

One potential approach to address the rising threat of antibiotic resistance is through novel formulations of established drugs. We designed antibiotic cross-linked micelles (ABC-micelles) by cross-linking the Pluronic F127 block copolymers with an antibiotic itself, via a novel one-pot synthesis in aqueous solution. ABC-micelles enhanced antibiotic encapsulation while also reducing systemic toxicity in mice. Using colistin, a hydrophilic, potent ″last-resort" antibiotic, ABC-micelle encapsulation yield was 80%, with good storage stability. ABC-micelles exhibited an improved safety profile, with a maximum tolerated dose of over 100 mg/kg colistin in mice, at least 16 times higher than the free drug. Colistin-induced nephrotoxicity and neurotoxicity were reduced in ABC-micelles by 10-50-fold. Despite reduced toxicity, ABC-micelles preserved bactericidal activity, and the clinically relevant combination of colistin and rifampicin (co-loaded in the micelles) showed a synergistic antimicrobial effect against antibiotic-resistant strains of Escherichia coli, Pseudomonas aeruginosa, and Acinetobacter baumannii. In a mouse model of sepsis, colistin ABC-micelles showed equivalent efficacy as free colistin but with a substantially higher therapeutic index. Microscopic single-cell imaging of bacteria revealed that ABC-micelles could kill bacteria in a more rapid manner with distinct cell membrane disruption, possibly reflecting a different antimicrobial mechanism from free colistin. This work shows the potential of drug cross-linked micelles as a new class of biomaterials formed from existing antibiotics and represents a new and generalized approach for formulating amine-containing drugs.

A thermodynamic study of F108 and F127 block copolymer interactions with liposomes at physiological temperature

The interactions of egg yolk phosphatidylcholine liposomes with F108 and F127 triblock copolymers, in the monomer state, were analyzed by isothermal titration calorimetry (ITC) at 37 °C. According to the results, the critical micelle concentration was determined to be 0.4 and 0.04 wt.% for F108 and F127, respectively, by surface tension at 37 °C. According to the results, liposomes/poloxamers were not favoured energetically, since endothermic interactions were observed. However, positive changes in entropy promoted a spontaneous process. F127 had a greater partition coefficient (51.97 ± 1.77 × 104), stronger affinity, than F108 (8.19 ± 0.37 × 104) towards the vesicle lipid bilayer due to its larger hydrophobic block. After the ITC experiments, an increased vesicle size (within about 1–3 nm average) by dynamic light scattering and the formation of bilayer discs by electron microscopy (EM) was observed at low copolymer concentrations (0.57 mol% of F108 and 1.01 mol% of F127). The EM and ITC results confirmed the intimate association of the copolymers with the membrane instead of being simply absorbed onto the bilayer surface. Our results indicate that the temperature of the system (37 °C), the copolymer concentration and hydrophobic chain length are important factors for the interaction of poloxamers with lipid bilayers and the stability of liposomes.

Silver/silver halide supported on mesoporous ceria particles and photo-CWPO degradation under visible light for organic compounds in acrylonitrile wastewater.

Silver/silver halide supported on ordered mesoporous ceria particles (Ag/AgCl/CeO2) were rapidly prepared by microwave-assisted soft template method, deposition precipitation method and photoreduction method, using cerium nitrate and silver nitrate as raw materials and block copolymer F127 as a template. The morphology, structure and chemical composition of the catalyst were characterized by XRD, SEM, EDS, TEM, N2 adsorption–desorption and UV-Vis Drs. Catalytic wet peroxide system assisted with visible light photocatalysis (photo-CWPO) was conducted to investigate the performance of organics degradation by Ag/AgCl/CeO2 as a catalyst in acrylonitrile wastewater. The results showed that the Ag/AgCl/CeO2 prepared has an ordered mesoporous structure, Ag and AgCl are formed on the surface of CeO2, with a specific surface area of 302.6–336.2 m2 g−1 and the average pore size is 8.04–8.90 nm. There is a strong absorption in the visible region and a band gap of 2.9 eV. The Ag/AgCl/CeO2 catalyst has higher catalytic performance in the photo-CWPO system than in the CWPO system alone. Ag loading, catalyst and H2O2 dosage, and pH value can affect the COD removal. When the concentration of COD in acrylonitrile wastewater was 500 mg L−1, the amount of catalyst was 200 mg, the amount of H2O2 (30%) was 8 mL, and the reaction time was 60 min, the COD removal reached 90%.

Resveratrol loaded polymeric micelles for theranostic targeting of breast cancer cells.

Treatment of breast cancer underwent extensive progress in recent years with molecularly targeted therapies. However, non-specific pharmaceutical approaches (chemotherapy) persist, inducing severe side-effects. Phytochemicals provide a promising alternative for breast cancer prevention and treatment. Specifically, resveratrol (res) is a plant-derived polyphenolic phytoalexin with potent biological activity but displays poor water solubility, limiting its clinical use. Here we have developed a strategy for delivering res using a newly synthesized nano-carrier with the potential for both diagnosis and treatment.Methods: Res-loaded nanoparticles were synthesized by the emulsion method using Pluronic F127 block copolymer and Vitamin E-TPGS. Nanoparticle characterization was performed by SEM and tunable resistive pulse sensing. Encapsulation Efficiency (EE%) and Drug Loading (DL%) content were determined by analysis of the supernatant during synthesis. Nanoparticle uptake kinetics in breast cancer cell lines MCF-7 and MDA-MB-231 as well as in MCF-10A breast epithelial cells were evaluated by flow cytometry and the effects of res on cell viability via MTT assay.Results: Res-loaded nanoparticles with spherical shape and a dominant size of 179±22 nm were produced. Res was loaded with high EE of 73±0.9% and DL content of 6.2±0.1%. Flow cytometry revealed higher uptake efficiency in breast cancer cells compared to the control. An MTT assay showed that res-loaded nanoparticles reduced the viability of breast cancer cells with no effect on the control cells.Conclusions: These results demonstrate that the newly synthesized nanoparticle is a good model for the encapsulation of hydrophobic drugs. Additionally, the nanoparticle delivers a natural compound and is highly effective and selective against breast cancer cells rendering this type of nanoparticle an excellent candidate for diagnosis and therapy of difficult to treat mammary malignancies.

Nanocatalytic Medicine of Iron-Based Nanocatalysts

Iron can be found in all mammalian cells and is of critical significance to diverse cellular activities within human bodies. Widespread applications and the underlying chemical and biological funda...

Polymer directed synthesis of NiO nanoflowers to remove pollutant from wastewater

Nickel oxide (NiO) nanoflowers are synthesized via a one-pot method using an amphiphilic block copolymer in aqueous solution. Pluronics F-127 block copolymer works as a structure-directing agent in the formation of the NiO nanoflowers. The controlled hydrolysis of the precipitating agent slowly releases ammonia that can form Ni(OH)2, which is stabilized in the polymer solution. The calcination removes the polymeric part of the nanocomposite and converts Ni(OH)2 into NiO with a face-centered cubic (FCC) phase. The synthesized NiO nanoflowers possess a mesoporous structure with an average surface area of 154 m2/g. Physisorption and electrostatic interactions between negatively charged congo red (CR) and positively charged NiO nanoflowers allow the adsorption of CR dye at ambient conditions. The adsorption of dyes follows pseudo-second-order kinetics, and the adsorbents are regenerated by calcination and recycled three times at similar efficiencies.

Alkaline activation of marble-like carbon structure and it’s application for inflammatory adsorption

For the first time, carbon microspheres successfully synthesized by using block copolymer F127 combined with gelatin, sucrose, and H2SO4 as soft template, source carbon, catalyst, respectively. The following step of synthesis are hydrothermal treatment, evaporation, carbonization and pyrolysis treatment under nitrogen flow. Microspheres carbon results have activated by a 10% KOH solution at room temperature for 12, 24, and 48 h, respectively then characterized by SEM and FTIR. The Activated microspheres carbon have used for ibuprofen adsorption. The characterization results showed that carbon microspheres carbon as marbles-like morphology with a diameter of 1-10 μm completed by C-OH, CO2, C≡N, -CNN, C=O, COO-, C=C,CK functional groups as the most. So this study shows that increasing activation time of the microsphere carbon have enhanced the equilibrium time and which is reach equilibrium at range 15-25 min and adsorption capacity range at 55.1-59.9 mg g−1. So carbon microspheres in general conclusion could be potentially as Drug Delivery material.