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A. Drying
The most common method for preserving plant material is drying. Enzymic processes take place in aqueous solution. Rapid removal of the water from the cell will, therefore, largely prevent degradation of the cell constituents. Drying also decreases the risk of external attack, e.g. by moulds. Living plant material has a high water content: leaves may contain 60-90% water, roots and rhizomes 70-85%, and wood 40-50%. The lowest percentage, often no more than 5-10%, is found in seeds.
To stop the enzymic processes, the water content must be brought down to about 10 %. Drying must be done quickly, in other words at raised temperatures and with rapid and efficient removal of the water vapor. The most efficient drying is achieved in large driers of the tunnel type. The plant material is spread out on shallow trays, which are placed on mobile racks and passed into a tunnel where they meet a stream of warm air. The air temperature is kept at 20-40 C for thin materials such as leaves, but is often raised to 60-70 C for plant parts that are harder to dry, e.g. roots and barks.
When the crude drug has been collected under primitive conditions, without access to a drier, it must be dried in the open. Even then, the material should be spread out in shallow layers with good ventilation to facilitate the drying. The choice of sunshine or shade is determined by the sensitivity to light of the constituents. In a dried drug the enzymes are not destroyed but only rendered inactive due to the low water content. As soon as water is added, they become active again. Hence, dried drugs must be protected from moisture during storage.
B. Freeze-drying Freeze-drying (lyophilization) is a very mild method. Frozen material is placed in an evacuated apparatus which has a cold surface maintained at -60 to -80 C. Water vapor from the frozen material then passes rapidly to the cold surface. The method requires a relatively complicated apparatus and is much more expensive than hot-air drying. For this reason, it is not used as a routine method, but it is very important for drying heatsensitive substances, e.g. antibiotics and proteins.
Methods of drying
Drying is carried out either by natural or artificial methods. 1- Natural drying: this is accomplished by natural air in sun or shade. 2- Artificial drying: this is a rapid method done at well-controlled temperature and is accomplished by: direct fire. Use of heated stones. Use of stoves.
C. Stabilization
On long storage, enzymic reactions will slowly destroy the constituents, because the last traces of water can never be removed. In order to avoid this degradation, the enzymes should be destroyed before drying, a process usually called stabilization.
The most common method being brief exposure (a few minutes only) of the plant material to ethanol vapor under pressure (0.5 atm). Stabilization may be of value for the isolation of compounds that are very susceptible to enzymic degradation.
D. Fermentation
Enzymic transformation of the original plant constituents is sometimes desirable. The fresh material is then placed in thick layers, sometimes covered and often exposed to raised temperatures (30-40 C) and humidity, so as to accelerate the enzymic processes. (This treatment is
usually called fermentation).
The fermented product must, of course, be dried afterwards to prevent attack by microorganisms, e.g.
moulds.
Fermentation is mostly used to remove bitter or unpleasant-tasting substances or to promote the formation of aromatic compounds with a pleasant smell or taste.
Where possible, temperature and humidity should be controlled to avoid damage to the active chemical constituents. The method and temperature used for drying may have a considerable impact on the quality of the resulting medicinal plant materials.
For example, shade drying is preferred to maintain or minimize loss of color of leaves and flowers; and lower temperatures should be employed in the case of medicinal plant materials containing volatile substances
The drying conditions should be recorded. In the case of natural drying in the open air, medicinal plant materials should be spread out in thin layers on drying frames and stirred or turned frequently. In order to secure adequate air circulation, the drying frames should be located at a sufficient height above the ground. Efforts should be made to achieve uniform drying of medicinal plant materials to avoid mold formation
Drying medicinal plant material directly on bare ground should be avoided. If a concrete or cement surface is used, the plant materials should be laid on a tarpaulin or other appropriate cloth or sheeting. Insects, rodents, birds and other pests, and livestock and domestic animals should be kept away from drying sites.
For in-door drying, the duration of drying, drying temperature, humidity and other conditions should be determined on the basis of the plant part concerned (root, leaf, stem, bark, flower, etc.) and any volatile natural constituents, such as essential oils. If possible, the source of heat for directs drying (fire) should be limited to butane, propane or natural gas, and temperatures should be kept below 60 C
If other sources of fire are used, contact between those materials, smoke, and the medicinal plant material should be avoided.
Packaging of Powders
Mixing of Powders
Large particles take a longer time for complete extraction than small ones and large differences in particle size thus slow down the extraction process. Several types of machines are available for grinding crude drugs: 1. Hammer mill; a common type for grinding crude drugs. 2. Knife mill; is useful for production of low-dust powders of leaves, barks and roots for subsequent percolation or maceration. 3. Tooth mill; is used for production of very fine powders.
Grinding produces a certain amount of heat which must be observed when grinding crude drugs containing heat-sensitive compounds. Mills cooled with liquid nitrogen are available for such purposes.
Cold grinding is also preferable for crude drugs containing volatile oils.
Following grinding, the material must be sifted to ensure the proper particle size. Sifting can be performed according to two different principles: sieving and blast sifting.
Sieving
In sieving the material is passed through a sieve of suitable mesh size giving two fractions. The fraction passing the sieve consists of particles with a size smaller than or corresponding to the mesh size. The remaining fraction consists of coarser particles which are returned to the mill for continued grinding.
Blast sifting
In blast sifting the material to be classified is blown with compressed air into an apparatus which allows the particles to sediment according to their weight. Coarse, heavy particles settle fast whereas small, light particles stay for a long time in the air stream.
sieves
SIEVE
SIEVE
SIEVE NUMBER
SIEVE OPENING
NUMBER OPENING
2.0 3.5 4.0 8.0 10.0 20.0 30.0 40.0 50.0 60.0
9.50 mm 5.60 mm 4.75 mm 2.36 mm 2.00 mm 850.00 um 600.00 um 425.00 um 300.00 um 250.00 um
70.0 80.0 100.0 150.00 um 120.0 125.00 um 200.0 75.00 um 230.0 270.0 325.0 400.0 63.00 um 53.00 um 45.00 um 38.00 um
212.00 um 180.00 um
Very coarse (No.8) Coarse (no. 20) Moderately coarse (No. 40) Fine (No. 60) Very Fine (No. 80)
Coarse (No. 20) Moderately coarse (No. 40) Fine (No. 80) Very Fine (No. 120)
Persyaratan WHO
Size of cut Medicinal plant materials are used either whole, or in cut or powdered form. Cut medicinal plant materials are prepared by cutting or crushing the plant into small pieces. The cut is graded according to the aperture size of the mesh of the sieve through which the material will pass, and is indicated as follows: Aperture size (mm) coarse cut 4.00 medium cut 2.80 fine cut 2.00
Sieves
The wire sieves used to sift powdered medicinal plant materials are classified by numbers that indicate their nominal aperture size expressed in m. The sieves are made of wire of uniform circular cross-section,
Sieves
SEDIMENTATION RATE, in which particles is determined by measuring the terminal settling velocity of particles through a liquid medium in gravitational or centrifugal environment (range: 0.8-300 micrometers)
Light Energy diffraction, in which particle size is determine by the reduction in light reaching the sensor as the particle, dispersed in a liquid or gas, passes through the sensing zone (range: 0.2 - 500 micrometers)
Laser halography, in which a pulsed laser is fired through an aerolized particle spray and photographed in three dimension with a halographic camera, allowing the particles to be individually imaged and sized (range: 1.4 100 micrometers)
Cascade Impaction is based on the principle that a particle, driven by an airstream, will impact on a surface in its path, provided that its inertia is sufficient to overcome the drag force that tends to keep it in the airstream
SIEVING particles are passed by mechanical shaking through a series of sieves (from 40 to 9500 micrometers, depending upon sieve sizes)
MICROSCOPY particles are sized through the use of calibrated grid background or other measuring devise ( range 0.2 to 100 micrometers)