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Rotary evaporator re301

Manufactured by Yamato Scientific
Sourced in Japan

The Rotary Evaporator RE301 is a laboratory equipment used for the efficient removal of solvents from liquid samples through the process of evaporation. It operates by rotating the sample flask while applying heat and reduced pressure, allowing the solvent to evaporate and be condensed for collection.

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3 protocols using rotary evaporator re301

1

Extraction and Yield Quantification of G. lotoides Seeds

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Freshly collected matured seeds of G. lotoides were thoroughly washed with tap water to eliminate any contaminants. After complete drying of the sample sunshade, it was pulverized by an electrical grinder. The dry powdered seeds of G. lotoides were subjected to extraction employing. One kg sample was soaked in a total of 5.7 litter of 80% hydromethanol with continuous shaking employing automatic shaker (Stuart Scientific) at 120 rpm at room temperature for 72 h. Then, the solution was primarily filtered employing muslin cloth and then refiltered with Whatman filters paper No.1. The marc was re-soaked with the same volume of solvents twice. Then subsequent filtrates were dried in to solid mass in a rotary evaporator (YAMATO rotary evaporator RE301, Japan, 40 °C, 60 rpm). The concentrated filtrate was subjected to deep freezer (DN-86W258) and then freeze-dried in a lyophilizer (Labfreeze Instruments Group Co., Ltd., Japan) at −50 °C. Ultimately, the %yield of extract was computed and kept at −4 °C using sealed container for experimentation [26 (link)].
The percentage yield of the rude extract %Yield= Seed extract weight obtained(g) Seed powder employed as stock×100
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2

Extraction of Persicaria maculosa Bioactives

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The leaf, stem and root samples of Persicaria maculosa plants were dried at 50˚C. Each type of sample was further ground and soaked in 96% v/v ethanol (1:10 ratio) at room temperature for 2 days. The extract was clarified through filter paper. The residue was further soaked in ethanol 96% v/v with the same ratio as above, repeated three times to ensure complete extraction [16] .
The extract was evaporated from the solvent using a rotary evaporator (Rotary Evaporator RE301, Yamato Scientific) at 40°C -55°C until about 50 mL of extract was obtained, which was poured into a beaker and allowed to evaporate naturally until concentrated. When the solvent was completely evaporated, the crude extract was collected and stored in the dark and at 4˚C for further experiments [16] .
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3

Ethanol Extraction of Leonotis nepetifolia

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The seperate parts of the Leonotis nepetifolia plant dried at 60°C until constant mass and then ground into fine powder. The powder was then soaked in absolute ethanol at a ratio of 1:3 (w/v) for 48 hours under room temperature. After soaking, the solution was clarified by filter paper to obtain the supernatant, and the residue continued to be soaked in alcohol as described above. The process was repeated again to ensure maximum recovery of the substances contained in plant powder. All volume of the ethanol extract was concentrated by using a rotary evaporator (Rotary Evaporator RE301, Yamato Scientific) to remove the solvent [20] . The extraction efficiency was defined as percentage by mass of extract relative to mass of original dry powder (w/w).
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