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Mpeg dspe

Manufactured by Laysan Bio
Sourced in United States

MPEG-DSPE is a lipid-based product used in the preparation of liposomes and other lipid-based formulations. It serves as a key component in the development of drug delivery systems and biomedical applications. The product provides a functional lipid moiety that can be incorporated into various lipid-based structures.

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11 protocols using mpeg dspe

1

Synthesis and Dispersion of C222 Graphene

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Example 9

C222 sample was synthesized following Simpson et al., reference 35, and, as above, was almost insoluble in any solvent. About 10 mg of this material was ground for 3 min. The resulting sample was then treated with oleum (about 20 ml) at room temperature for a day. After dilution of the acid to 500 ml solution, sodium carbonate was used to neutralize the solution. The resulting sample was centrifuged down from water solution at 5000 g for 15 min. Then the sample was transferred to DMF and sonicated using a bath sonicator in DMF (5 mL) solution of TBA (65 μl) for 15 mins. The suspension was put at room temperature for 3 days to let the TBA fully inserted into graphene layers. Then the suspension was bath-sonicated with DSPE-mPEG (Laysan Bio. Inc., Arab, Ala.) (15 mg) for 15 min., forming a homogeneous suspension. After centrifuging the suspension at 24000 g for 1 hr, a black suspension with C222 (dispersed by the surfactants, probably with sulfurate groups at the edges) retained in the supernatant was obtained.

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2

Synthesis of Single-Layer Graphene Sheets

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Example 6

Natural graphite flakes (Superior Graphite Co., ˜10 mg) were ground with NaCl crystallites for 3 mins forming a uniform grayish mixture. Small pieces of graphite flakes were separated and collected by dissolving NaCl with water and filtration. The resulting sample was then treated with oleum (about 5 ml) at room temperature for a day. After complete removal of acid by filtration and repeated washing, the resulting sample was ultra-sonicated using a cup-horn sonicator in DMF (10 mL) solution of TBA (130 μl) for 5 mins. The suspension was put at room temperature for 3 days to allow the TBA to fully be inserted into the graphene layers. Then, 5 mL of the suspension was taken out and bath-sonicated with DSPE-mPEG (Laysan Bio. Inc., Arab, Ala.) (15 mg) for lhr forming a homogeneous suspension. After centrifuging the suspension at 24000 g for 3 mins, we obtained black suspension with mostly single layer GS retained in the supernatant.

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3

Biocompatible SWNT Preparation

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High-pressure carbon monoxide conversion (HiPCO) SWNTs (Unidym, Inc.) were suspended in an aqueous solution of sodium deoxycholate at a concentration of 1 wt% by bath sonication for 1 h. This SWNT suspension was ultracentrifuged at 300,000 g, the supernatant was retained and 1.0 mg·ml−1 of DSPE-mPEG(5 kDa) (1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethyleneglycol, 5000)], Laysan Bio) was added. The resulting suspension was then dialyzed against 1× PBS in a 3500 Da membrane (Fisher) with pH controlled at 7.4 to remove sodium deoxycholate, leaving the SWNTs coated with the biocompatible DSPE-mPEG only.
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4

Graphene-coated Battery Cathode Powders

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DSPE-mPEG (0–0.2 wt.%, MW 5000, Laysan Bio), an amphiphilic surfactant, was added into 10 ml of the Gr dispersion (1 wt.% Gr in DMF) followed by 30 min of tip sonication, producing small Gr pieces. A total of 3 g of Ni-rich oxides (NCA and NCM811) or LCO powders were added to the Gr solution with a weight ratio of cathode powder:Gr solution = 1: 2. The solution was then subjected to vortex mixing for 5 min. The coated cathode powders were collected by centrifugation at 193 × g, followed by washing with ethanol to remove residual Gr and vacuum drying at 150 °C for 5 h. The coating process, including an intermediate 10 min drying step was repeated to enhance Gr coverage. Through controlled experiments, various surfactants/additives, such as Triton-X100 [(C14H22O(C2H4O)n); nonionic surfactant, Sigma-Aldrich], sodium dodecyl sulfate (CH3(CH2)11SO4Na; anionic surfactant, Sigma-Aldrich), cetyltrimethylammonium bromide ([(C16H33)N(CH3)3]Br; cationic surfactant, Sigma-Aldrich), and PVP (MW 10,000, Alfa-Aesar), were used to study the effect of surfactants on the Gr coating behavior, as compared with DSPE-mPEG.
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5

Single-Layer Graphene Sheets Preparation

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Example 1

The single layer graphene sheets (GS) preparation started by exfoliating expandable graphite (160-50N of Grafguard Inc.) at 1000° C. in forming gas for 60 s. Then exfoliated graphite (˜10 mg) was ground with NaCl crystallites for 3 mins forming a uniform grayish mixture. Small pieces of exfoliated graphite were separated and collected by dissolving NaCl with water and filtration. The resulting sample was then treated with oleum at room temperature for a day. After complete removal of acid by filtration and repeated washing, the resulting sample was ultra-sonicated using a cup-horn sonicator in DMF (10 mL) solution of TBA (130 μl) for 5 mins. The suspension was put at room temperature for 3 days to let the TBA fully inserted into graphene layers. Then 5 mL suspension was taken out and bath-sonicated with DSPE-mPEG (Laysan Bio. Inc., Arab, Ala.) (15 mg) for 1 hr forming a homogeneous suspension. After centrifuging the suspension at 24 kg for 3 mins, we obtained black suspension with mostly single layer GS retained in the supernatant.

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6

Lipid Nanoparticle Formulation Protocols

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DSPE-PEG2000 was from Laysan Bio, Inc. (mPEG-DSPE, molecular weight 2000, Arab, AL, USA). L-α-Phosphatidylcholine (from egg yolk) was from Sigma-Aldrich (Catalog No. P-2772, St. Louis, MO, USA). F12511 and K604 were custom synthesized by WuXi AppTec in Shanghai, China. Based on the HPLC/MS and NMR profiles, F12511 was 98% in chemical purity and in stereospecificity (F12511 contains an asymmetric center) [51 (link)] and K604 was 98% in chemical purity. CP113,818 was a research gift from Pfizer. [1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide] DiR (catalog #22070) was purchased from AAT Bioquest, Pleasanton, CA, USA.
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7

Lipid-based Nanoparticle Formulation

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DSPE-PEG2000 is from Laysan Bio, Inc (mPEG-DSPE, MW 2,000). L-a-Phosphatidylcholine is from Sigma-Aldrich (Catalog No. P-2772). F12511 and K-604 were custom synthesized by WuXi AppTec in China. Based on HPLC/MS and NMR profiles, purity of F12511 was 98% and in stereospecificity; purity of K-604 was 98% in chemical purity. Organic solvents are from Fisher Scientific.
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8

Lipid Characterization and Cell Line Cultivation

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Lipids including DBPC (1,2-dibehenoyl-sn-glycero-3-phosphocholine), DPPA (1,2 dipalmitoyl-sn-glycero-3-phosphate), and DPPE (1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine) were obtained from Avanti Polar Lipids (Pelham, AL), and mPEG-DSPE (1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000] (ammonium salt)) was obtained from Laysan Bio, Inc.(Arab, AL). Propylene glycol (PG) was purchased from Sigma-Aldrich (Milwaukee, WI). Glycerol was purchased from Acros Organics (Morris, NJ). Human ovarian cancer cells (OVCAR-3) and breast cancer cells (MCF-7) were purchased from ATCC (Manassas, VA). The Roswell Park Memorial Institute (RPMI) 1640 and Minimum Essential Media (MEM) enriched with 10% fetal bovine serum and 1% penicillin–streptomycin, trypsin–EDTA were purchased from Invitrogen (Grand Island, NY). The cell proliferation reagent WST-1 was purchased from Sigma-Aldrich (Milwaukee, WI). The cellular ROS fluorogenic dye (2′,7′-dichlorofluorescin diacetate or DCFDA) was purchased from Abcam (Cambridge, MA).
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9

Pheophorbide a Lipid Nanoparticle Formulation

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Pheophorbide a (PA) was bought from Santa Cruz Biotechnology (TX, USA). l-α-Phosphatidylcholine was purchased from Avanti Polar Lipids, Inc (AL, USA). Cholesterol was brought from MP Biomedicals (OH, USA). mPEG-DSPE (MW: 2000) was brought from Laysan Bio, Inc (AL, USA). Organic solvents were purchased from Fisher Scientific (MA, USA).
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10

Multimodal Nanoprobe Development for Cancer

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SPIONs (15 nm) were kindly donated by Prof. Shun Shen, Tongji University. PEPHC1 (C6-HFLIIGFMRRAACGA) peptide and 5-FAM-labeled PEPHC1 (5-FAM-C6-HFLIIGFMRRAACGA) peptide were synthesized by the Chinese Peptide Company (Hangzhou, China). EGFRvIII (D6T2Q) XPRabbit monoclonal antibody was purchased from Cell Signaling Technology (USA). Alexa Fluor 647-conjugated donkey-anti-rabbit secondary antibody was purchased from Abcam (USA). mPEG-DSPE (MW = 2000) and DSPE-PEG-NH2 (MW = 3400) was purchased from Laysan Bio (USA). DSPE-PEG-NHS (MW = 2000) was obtained from Nanocs (USA). DAPI (2-(4-amidinophenyl)-1H-indole-6-carboxamidine) was obtained from Beyotime (Nantong, China). Coumarin-6 was bought from Sigma (USA) and Cy7.5 NHS ester was purchased from Nanocs (USA). Fetal bovine serum (FBS), phosphate buffered saline (PBS), trypsin-EDTA (0.25%), high glucose Dulbecco’s modified Eagle’s medium (DMEM) and penicillin-streptomycin were purchased from Gibco (CA, USA). The MTT cell proliferation and cytotoxicity assay kit was obtained from Sigma (USA). Puromycin was purchased from Aladdin (Shanghai, China). All other reagents were of analytical grade and used without further purification.
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